236 Api Manufacturing Jobs - Page 9

We are looking for a dynamic and experienced General Manager to spearhead Sales and Marketing efforts within our CDMO markets at Chieron Active Ingredients. This pivotal role demands a seasoned leader capable of building and nurturing a robust CDMO business, leveraging extensive industry knowledge and contacts. The ideal candidate will possess a comprehensive understanding of the entire product development lifecycle, coupled with strong technical acumen and familiarity with global pharmaceutical regulations. This individual will collaborate closely with technical leaders, both internally and externally, to drive business growth. The role requires a strategic mindset, patience, and unwavering persistence, given the long sales cycles inherent in the CDMO sector. The General Manager will be responsible for developing and executing sales strategies, managing key accounts, ensuring regulatory compliance, and fostering innovation within the CDMO division. They will also play a crucial role in identifying and capitalizing on emerging pharmaceutical industry trends to maintain Chieron Active Ingredients' competitive edge. This is a high-impact position for a results-oriented professional eager to shape the future of our CDMO business. Job Details: Industry: Active Pharmaceutical Industry Department: Sales and Marketing (CDMO) Role: General Manager (Sales and Marketing for CDMO Markets) Location: Hyderabad Experience: 18 to 25 years Employment Type: Full-time Qualifications: Bachelor's or Master's degree in Chemistry, Pharmacy, or a related field. MBA preferred. Responsibilities: Strategic Leadership & Business Development Lead the development and execution of the CDMO sales and marketing strategy to achieve revenue targets and market share growth. Identify and evaluate new business opportunities within the CDMO landscape, including market trends, competitive analysis, and potential partnerships. Develop and maintain strong relationships with key decision-makers at target pharmaceutical companies. Oversee the preparation and presentation of compelling proposals and presentations to prospective clients. Monitor and report on market trends, competitor activities, and customer feedback to refine sales and marketing strategies. Represent Chieron Active Ingredients at industry conferences, trade shows, and networking events to enhance brand visibility and generate leads. Sales Management & Key Account Management Manage and mentor the CDMO sales team, providing guidance, training, and support to achieve individual and team goals. Develop and implement effective sales processes and tools to optimize sales efficiency and conversion rates. Oversee the management of key accounts, ensuring customer satisfaction and fostering long-term partnerships. Negotiate contracts and agreements with clients, ensuring favorable terms and conditions for Chieron Active Ingredients. Monitor sales performance metrics and identify areas for improvement, implementing corrective actions as needed. Collaborate with cross-functional teams to ensure seamless execution of CDMO projects and deliverables. Technical & Regulatory Compliance Maintain a thorough understanding of API manufacturing processes, pharmaceutical regulations (GMP, GLP), and quality standards. Ensure that all CDMO activities comply with relevant regulatory requirements and industry best practices. Collaborate with the technical and quality assurance teams to address client inquiries and resolve technical issues. Oversee the preparation and review of technical documentation, including CMC sections, regulatory submissions, and quality control reports. Stay abreast of changes in global pharmaceutical regulations and update internal processes accordingly. Participate in client audits and inspections, ensuring successful outcomes and maintaining a strong reputation for quality and compliance. Project Management & Cross-Functional Collaboration Oversee the project management of CDMO projects, ensuring timely completion, adherence to budget, and achievement of quality objectives. Collaborate with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs, to ensure seamless project execution. Communicate effectively with clients and internal stakeholders, providing regular updates on project progress and addressing any concerns. Identify and mitigate risks associated with CDMO projects, implementing contingency plans as needed. Track project performance metrics and identify areas for improvement in project management processes. Ensure that all project documentation is complete, accurate, and readily accessible. General Expectations and Past Experiences: Proven track record of successfully building and managing CDMO sales teams and achieving revenue targets in the pharmaceutical industry. Extensive knowledge of API manufacturing processes, pharmaceutical regulations (GMP, GLP), and quality standards. Demonstrated expertise in contract negotiation, strategic account management, and business development within the CDMO sector. Strong technical acumen and ability to communicate effectively with technical leaders, both internally and externally. Excellent communication, presentation, and interpersonal skills, with the ability to build rapport and influence key decision-makers. Experience in developing and implementing sales and marketing strategies to drive business growth in the CDMO market. Proficiency in project management methodologies and tools, with the ability to manage multiple projects simultaneously.

Operating and maintaining equipment Monitoring production processes Monitor production processes, identifying and reporting any issues Maintain accurate and complete records of production activities Ensuring adherence to quality standards and GMP Required Candidate profile Previous experience in API pharma manufacturing or a similar industry Ability to operate and maintain equipment Knowledge of GMP and other relevant regulations is essential

Ensuring the quality of APIs through testing, analysis, & documentation Sample & inspect raw materials Maintain an accurate & complete record of testing, analysis Investigate deviations from the quality standard Ensure compliance with GMP regulations Required Candidate profile Bachelor's degree in B.Sc/M.Sc Chemistry, B.Pharm/M.Pharm. Previous experience in QC in API pharma manufacturing Strong knowledge of analytical techniques & instrumentation, e.g., HPLC, GC, UV-Vis

Role & responsibilities You will be based at their Plant in Palghar Maharashtra. 1.He will be responsible for handling entire Production activities and will lead team including Officer , Executive , Worker and Contract Labour etc. 2. You will be responsible for handling all Production & Operational Activities at Plant level and will supervise /control Different teams. 3. He will be responsible for handling all Domestics & International Audits including USFDA , UKMHRA , EUGMP , ROW etc. 4. You will be closely co- ordinate with all other department for Smooth Plant Operation like a.Production and project Management b.. Quality/ Audit/Compliance c. Cost Reduction Initiatives d. Process Development / Technology Transfer e. Inventory Management f. Team Management g.Production and project Management 5. Proven abilities in commissioning the new product as per write up of R&D with gram scale to kilo scale and new plant establishment and new project, set up of various new equipment. Preferred candidate profile 1. Candidate should be B.Tech in Chemical Engg or M.Sc in Chemistry. 2. Candidate should have at least 18-20 years of working experience from any well-known USFDA approved API Bulk Drugs Company 3. You should good in team handling including Officer, Executive + Contract Labours. 4. You should be good in handling International Audits Like USFDA , UKMHRA , EUGMP , ROW etc. 5. You should be good in Man Management.

Role & responsibilities You will be based at API Bulk Drugs (USFDA Approved Plant) in Patalganga , Mahad Maharashtra. 1.He will be responsible for handling entire Production activities and will lead team including Officer , Executive , Worker and Contract Labour etc. 2. You will be responsible for handling all Production & Operational Activities at Plant level and will supervise /control Different teams. 3. He will be responsible for handling all Domestics & International Audits including USFDA , UKMHRA , EUGMP , ROW etc. 4. You will be closely co- ordinate with all other department for Smooth Plant Operation like a.Production and project Management b.. Quality/ Audit/Compliance c. Cost Reduction Initiatives d. Process Development / Technology Transfer e. Inventory Management f. Team Management g.Production and project Management 5. Proven abilities in commissioning the new product as per write up of R&D with gram scale to kilo scale and new plant establishment and new project, set up of various new equipment. 6. In the absence of Sr. GM Technical Operations, the You will be responsible for planning and authorizing all production-related activities. Preferred candidate profile 1. Candidate should be B.Tech in Chemical Engg or M.Sc in Chemistry. 2. Candidate should have at least 18-20 years of working experience from any well-known USFDA approved API Bulk Drugs Company 3. You should good in team handling including Officer, Executive + Contract Labours. 4. You should be good in handling International Audits Like USFDA , UKMHRA , EUGMP , ROW etc. 5. You should be good in Man Management.

Role & responsibilities production chemist Preferred candidate profile pharma experience, API, BULK DRUG,GMP, GLR,SSR,CENTRIFUSE,BPR,

Knowledge of preparation of BMR, BPR, MFR, SMP, Change control, Deviation. Develop and implement quality assurance system Oversee quality control process Conduct internal audits & inspections Ensure laboratory compliance with regulatory requirements Required Candidate profile Bachelor's degree in a relevant scientific field like B.Pharma, M.Pharma, B.Sc Previous experience in quality assurance in laboratory setting or an API Mfg company Min 5 years of experience required

Hii, Greetings from Avaniconsulting ! We are hiring immediate joiners for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 5-10 yrs in API Notice Period - 1 month ( maximum) / immediate joiners Location - Mysore ( Nanjangud) Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical Salary- 20% to 30% hike on current ctc Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. if interested kindly share their updated resume with below details to priyanka@avaniconsulting.com or whatsapp to 9518220852 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change:

JOB OPENING FOR API API MANUFACTURING 1. Role: Sterile- Autoclave, Compounding, Crystallization & Filling Experience: 5 to 12 years Education: B. Sc/M.Sc Chemistry/B.Pharm/M. Pharm Job Description: 1. Handling of Autoclave, DHS, Canister washing machine, Crystallizer, ANFD, Co-mill, Sterile batch mixture and filling machine. 2. Well versed knowledge of sterile process and Media fill, filter integrity machine, NVPC Machine 2. Role: Sterile- Shift Incharge Experience: 6 to 12 years Education: B. Sc/M.Sc Chemistry/B.Pharm/M. Pharm Job Description: 1. Well versed knowledge in Validation, Qualification, Media Fill, SAP activity, change control, Deviations, CAPA, Investigations and other QMS related activities, Filter intrigity Machine, NVPC Machine. 2. Exposure in Regulatory inspection audits 3. Role: Non-Sterile Experience: 2 to 8 years Education: B.Sc/M.Sc(Chemistry)/B E/B.Tech(Chemical) Job Description: 1. Handling of Hydrogenation reaction. 2. Handling all type of equipments.. Reactor, Sparkler Filter, Centrifuge, VTD, FBD, etc 4. Role: Non-Sterile (Shift Incharge) Experience: 5 to 10 years Education: B.Sc/M.Sc(Chemistry)/B E/B.Tech(Chemical) Job Description: 1. Well versed knowledge in Validation, Qualification, Media Fill, SAP activity, change control, Deviations, CAPA, Investigations and other QMS related activities. 2. Knowledge of Clean room. 5. Role: Documentation Experience: 5 to 10 years Education: B.Sc/M.Sc(Chemistry)/B E/B.Tech(Chemical) Job Description: 1. Well versed knowledge of change control, Deviations, Investigation, QMS and cGMP. 2. Preparation and revision of MFR or MPR, BMR or BPR, SOPs, Trend, Qualification, Validation related documents, Protocol and reports 4. Well versed knowledge of SAP system. API WAREHOUSE 1. Experience: 5 to 8 years Education: B.Sc/M.Sc(Chemistry)/B E/B.Tech(Chemical) Job Description: 1. Oversee the receiving, storage, and distribution of raw materials, packaging materials, intermediates, and finished products. 2. Well knowledge in SAP activity 2. Experience: 6 to 10 years Education: B.Sc/M.Sc(Chemistry)/B E/B.Tech(Chemical) Job Description: 1. Coordinate with procurement, production, and logistics teams to ensure timely and accurate delivery of materials. 2. Knowledge in SAP activity. 3. Activities comply with GMP, GDP and other regulatory requirements. API QA 1. QMS Experience: 4 to 7 years Education: M.Sc(Analytical Chemistry)/M.Pharma Job Description: 1. Preparation of SOP, Specification, STP, ARDS, Protocol, Reports, Stability summary report, Miscellaneous document and analytical method validation inline of applicable pharmacopoeia and ICH guideline. 2. Handling of QMS related activity i.e OOS, OOT, Deviation, OOC, Change control and CAPA 2. Validation Experience: 2 to 5 years Education: M.Sc(Analytical Chemistry)/M.Pharma Job Description: 1. Knowledge of preparation, review & compilation of qualification and validation documents. 2. Handling and preparation of regulatory audits 3. To prepare and review Computer System Validation Master Plan document. 3. IPQA Experience: 2 to 5 years Education: M.Sc(Analytical Chemistry)/M.Pharma Job Description: 1. Monitor, assess, and validate ongoing manufacturing processes, ensuring compliance with regulatory requirements, internal SOPs, and GMP. 2. Perform investigation and resolution of any quality issues and document any process deviations and implement corrective action.

Role & responsibilities For Trainee - 1Year RM Issuance and Charging activities Monitoring activities during manufacturing Final Product patching activities For 2-3 Years Shift production activities Packing activities Comply GDP/GMP/ Safety Preferred candidate profile Male Candidates from Chennai and Tamilnadu (Tamil Speaking ) with sound subject knowledge (Chemistry) for fresher and API Manufacturing Industry background for experience preferred. We require immediate joiners. Flexible for working in shifts Perks and benefits As per Industry standard

1. Experience in API / Intermediates manufacturing company 2. Working as per SOP and follow the safety protocols 3. Working experience in GMP environment 4. Maintaining Documentation / BMR

Hello, Greetings for day! Please find the below JD Preparation/ review of standard operating procedure (SOP), calibration procedures, specifications, standard test procedures, general test procedures etc. Conducting training on specification and method of analysis, SOPS and calibration procedures. Handling of QMS documents like Change control, CAPA, Incidents, OOS, deviations, Out of calibrations, OOT etc. To ensure timely closure of documents like Change control, CAPA, Incidents, OOS, deviations, Out of calibrations, OOT etc. To investigate the laboratory error / incident and its impact on quality and analysis of all samples. Participating as a cross functional team member for investigation of any QMS related issues. To observe and maintain Good Laboratory Practices. To prepare / review documents like stability schedule, hold time study schedule, preventive maintenance schedule, calibration schedule. Co-ordination with outside calibration agencies. To prepare/review instrument qualification data. Coordinating with other departments for smooth functioning of laboratory. Arranging standards required for the analysis. Arranging columns required for analysis. To approved sign in TRF( Intermediate) ,GRN,Hold time sample, stability sample Ensuring training of departmental staffs as per job requirement. Attending training program as per CGMP training schedule. To take part in method validation/transfer/verification activity. To maintain discipline in the laboratory. To prepare the analysis request form and send the sample to contract laboratory for analysis. To take part in customer/regulatory/internal audits. Responsible for follow the health, safety & environment norms as per company policy & procedures. To monitor the good housekeeping practices in all quality control area. To co-operate in achieving the quality control objective. Preferred candidates should be form CDMO industry or somebody who has handled multiple API product and handled 50 members team. Interested candidates can share their update resume and below details on 'jyotsna.sable@aartipharmalabs.com' Total years of exp: Current CTC Exp CTC: Notice Period: Are you open for move to Gujarat: Do you have experience in CDMO/API Manufacturing Industry: what is the team size did you handle?

The Quality Control Chemist is responsible for developing and implementing quality control procedures and standards, monitoring and inspecting product quality to ensure compliance with established standards, analyzing test results . Required Candidate profile 1. Must have experience in QC Lab / Validations. 2. Must have B.Sc. / M.Sc. Organic Chemistry. 3. Must have 01- 05 Years of experience in QC Labs. Perks and benefits Free Bus , ESI , PF , Subsidized Canteen Food .

Carry out the manufacturing operations according to the BPCR provided by QA department Perform the Operations in accordance to the established SOPs and cGMP. To maintain for Good documentation practice .To execute Production planning schedule. Required Candidate profile < Qualification : B.sc /M.sc(Chemistry)/B. Pharmacy/B. Tech ( Chem engg) - Any chemistry Background. < Having Pharma Experience of 2- 8 Years of experience. Perks and benefits Free Bus , Canteen, Pf

Hii, Greetings from Avaniconsulting ! We are hiring for Production associate for a leading Pharma API Manufacturing company Position- Associate Work Experience Min 3-10 yrs in API Notice Period - 1 month ( maximum) Location - Mysore ( Nanjangud) Gender - Any Qualification- B.Tech in Chemical Engineering /Msc Chemistry/Diploma Chemical Salary- 20% to 30% hike on current ctc Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team while in the department. 3. To ensure adherence of process instructions as per Batch Manufacturing Record and respective departmental procedures. 4. To ensure good housekeeping in the production shop floor. 5. To ensure compliance to cGMP, Safety, Health & Environment in delivering the product of intended Quality. 6. To ensure batch records on completion are reviewed for adequacy prior to hand over to QA for review, compliance & release / rejection. 7. To report deviations / incidents immediately upon occurrence and to conduct investigation in coordination with cross functional teams. 8. To ensure all document entries are performed online with legible, errors corrected with signature and date. 9. Monitoring and control of manufacturing environment and filling of daily log books. 10. To ensure preventive maintenance of equipment, calibrations of gauges / instruments are performed as per schedule & the outcome of verification is within control. 11. To ensure the sanitization activity is performed in the department. 12. To support QA in investigations related to OOS, Deviations, CAPA, Incidents, complaints or recalls, validations and any other support that would be required. 13. To ensure the raw material / Intermediates / API(s) are labelled at each stage of process and stored with appropriate segregation at recommended storage conditions ensuring no impact on product Quality. 14. To ensure that stocks are reconciled at regular intervals. 15. Any other assignment allocated by Production head. if intrested kindly share their updated resume with below details to jyotsna@avaniconsulting.com or whatsapp to 7780363938 1. Current CTC: 2. Expected CTC: 3 . Notice Period: 4. Total Experience 5. Current Location: 6. Preferred Location: 7. Reason for change:

Manage all aspects of pharmaceutical production operations, including scheduling, resource allocation, and quality control, ensuring compliance with regulatory requirements. Develop and implement production plans to meet demand forecasts while optimizing efficiency and minimizing costs Organize, supervise and implement and achieve production targets in accordance with cGMP, safety and productivity Implementing cost saving measures to achieve substantial reduction in terms of raw materials, manpower and increased machine utilization Waste elimination in manufacturing system and Collaborate with cross functional teams, R&D, quality assurance, and supply chain, to drive continuous improvement initiatives and resolve production issues. Maintaining the Standards of Plant & Documentation with respect to regulatory expectations

Role: Production Chemist & QC Chemist Exp: 1+ Yr (Into Pharma Industry only ) Sal: 25% Hike on CTC Loc: Bollaram Qual: BSc/MSc/Bpharma Gender: Males/Females * API Manufacturing CONTACT SRUTHI 8125254983 3ghr33@gmail.com

Position: Production Head / Manager Education: BSc. in chemistry, MSc. in chemistry or B.pharma / M.Pharma Experience: minimum 10 year in API pharmaceutical industries. Salary: 50 to 70 K per month Mo No : +91 90816 99400 / +91 90816 88100 Required Candidate profile Coordinate with regulatory authorities for inspections, licensing, and compliance documentation. Investigate quality incidents, deviations, and complaints, ensuring timely resolutions

Industry:- Pharma / Chemical /ETP Location :-Surat / Vadodara/ Navsari /Bharuch Qualification :-Bsc/M.sc Chemistry Experience :- 2-5 year Post :- Production QA/RA/QC Chemist Salary :20 k to 40 k CTC Male / Female Required Job Time : 9 am to 6 pm Required Candidate profile Perform In-Process Quality Control (IPQC) during tablet MFG. compliance with cGMP,coordinate with QA, QC, and Maintenance. +91 90816 99400 / +91 90816 99600 /+91 90816 99500

Production Chemist required for a pharma company at kundli, sonipat Qualification- B. pharma Exp- min 7 yrs salary- upto 60k Wtsapp me resume at 8295842337- MR. Bansal

Position: Production Executive/Sr. Executive (Total 10 Vacancies) Industry: API Manufacturing Experience: 4-7 years in cGMP API manufacturingin the Production Department. Qualifications: B.Sc/ M.Sc/ B.E. in Chemical Job Description: Responsible for overseeing all production activities in API manufacturing, ensuring adherence to cGMP, regulatory compliance (USFDA, EU, MHRA), and safety protocols. Maintain batch records, SOPs, and production-related documentation per regulatory requirements. Monitor process parameters, equipment operation, and material management to ensure efficiency and quality. Coordinate with cross-functional teams for audits, validations, and deviations. Implement continuous improvements, conduct training for shop-floor personnel, and ensure strict compliance with EHS guidelines. Troubleshoot production issues, ensure timely completion of batches, and support technology transfers. Maintain discipline and productivity, ensuring alignment with organizational and regulatory expectations.

Job Responsibilities are not limited: Overall responsibility of raw material, finished goods & engineering stores. To ensure the receipt and proper storage of material. The safe practices in Stores. Must have the knowledge of MSDS & other EHS. Required Candidate profile Knowledge of NDPS Act, GST and Excise is must. Develop the talent of self & team in the WH related activities primarily. To maintain practices, records & systems as per cGMP.

Sourcing of KSMs, intermediates and MRO items for API Manufacturing Plant . New vendor Development and vendor Qualification, arranging all regulatory support/technical support from vendor as per requirement of RA/QA/CQA). Procurement of Raw material, solvents (Bulk), Bulk commodity items for API plants. Obtaining best prices for imports/domestics from Vendors & Cost Cutting through negotiation with suppliers (domestic/foreign). Co-ordinating with CHA agent for the material Imports, custom clearance, and Documentation. Responsible for tracking & timely delivery of Raw materials to API plants. Managing day-to-day functioning of purchasing Group / Department. Support & Coordinating with the various Departments for Procurement of Raw Materials, R&D materials, Common Materials & Packaging Materials. Vendor Analysis & Development of new Vendors. Accountable for Raw & Packing material requirement and availability, in line with production plan. Responsible for floating of purchase enquiries and Purchase orders. Maintaining effective record keeping on all purchase orders and supplier confirmations. Working with Suppliers on Lead Time Reduction. Follow up with Vendor for delivery and to get the material at the right time and required quantity. Responsible for site transfer of Raw material and Packing material. compliance guidelines of USFDA and Standard Operating Procedures. Knowledge of Change controls, Deviations and CAPAs related to Material and Purchase. Inventory Control and Purchase Planning. Floating of purchase enquiries/orders. Management and Coordination with Production, Logistic & warehouse Dept. Responsible for constant check on stock levels. Good knowledge of Excel and Presentation

Sun Pharmaceutical Industries Ltd. Position: Senior Manager API Production (Block Head) Grade: G9B Location: API Ahmednagar - Production Planning and scheduling (day to day basis) - Ensuring resources available (BMR, Raw Material Manpower etc.) Liaison with QC/QA/STORE/Eng. Dept. for solving of trouble shooting problem. - Implementation and monitoring of GMP Standard. - Introduction and scale up of technology transfer. (New Prod 1ct) Constantly monitoring and improvement of product process, efficiency, services etc. - Documentation work, Monthly Report, data preparation (Process trend analysis) and root cause analysis. - Ensure the availability of consumable items & Planning of RM require as per campaign basis. - Ensure the documents related to process I cleaning / House Keeping. Control on fresh as well as recovered solvents/ spent solvent. - Ensure the solid and process waste transfer to respective area and record maintaining. - Other activities entrusted from time to time. Review the prepared/ Revision of BMR and SOP. - Operation of electronic system i.e.ONE HR portal, Metis Track wise, Minitab, Out Look etc. - Ensure Preventive Maintenance of Plant Equipment's in time frame. Ensure the training to subordinates. - Extended Facility of reactor Area of Plant-06 production Planning and scheduling (day to day basis)

To support the development of scalable fermentation processes from shake flask to 25000 litre reactor scale. To support the process development and scale-up operations from laboratory to plant scale. To support the set-up, operate and monitor microbial fermentation processes under batch, fed-batch and continuous conditions following protocols To work in partnership with colleagues to modify or reconfigure vessels and associated equipment to define the process parameters necessary to achieve optimal. To support the routine maintenance of fermenters, identifying and escalating issues which may impact their performance and availability. To support the design of experiment (DOE) to study the effect of multiple variables on fermentation performance and the effects of interactions between variables To be responsible for providing clearly documented records of technical data, decisions, methodologies, calculations, and software use in an agreed format. To support with internal and external customers as required identifying and understanding their needs and contributing to the design and delivery of agreed outcomes within agreed timescales. To share professional knowledge with colleagues and be responsible for own continuous professional development.