321 Injectables Jobs

Vaccine Manufacturing (Cell Culture) Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in handling Roller bottles, Cell stacks, TCFs. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCFs. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Quality Control Analyst Biochemical techniques, Chromatography techniques, Electrophoresis techniques, Immuno assay techniques Cell culture techniques, Molecular techniques Analytical method validation (AMV), Analytical Method Development and Transfer Quality control (QC), cGMP, cGLP and QMS. Drug Product (Filling-Officer/Executive/Sr. Executive/Operator) Experienced in handling of O-RABS, Operation of Vial washing/Filling/Lyophilizers/Autoclave/Process vessels.

Please send me your cv on 8982382014 and Poorvi.tiwari@adecco.com Injectable Operator Aseptic Area Manufacturing Job Title: Operator Aseptic Area Manufacturing Category: Operator Location: Ahemdabad Experience Required: 57 Years Qualification: Diploma in Engineering / ITI Role Summary: We are seeking experienced Operators for our Aseptic Area Manufacturing operations. The ideal candidates will have a strong background in operating and maintaining critical aseptic area equipment to ensure smooth and compliant manufacturing processes. Key Responsibilities: Operate and monitor aseptic area filling machines and sealing machines. Perform ALUS (Automated Loading and Unloading System) operations efficiently. Handle storage vessels including their operation, monitoring, and routine cleaning. Maintain cleanliness and aseptic conditions in the production area as per GMP guidelines. Carry out line clearance, changeovers, and batch-wise documentation. Support preventive maintenance and minor troubleshooting of equipment. Adhere strictly to SOPs, quality standards, and safety regulations. Required Skills: Proficient in handling aseptic equipment including: Filling Machines Sealing Machines ALUS Systems Storage Vessels

Please share you cv in below email ID with updated cv on renu.kumari@adecco.com Watsapp :8758695449 To supervise all activities in parenteral department, Visual inspection area, external vial washing and freeze dryer technical area activities. To supervise all activities in oncology parenteral department, Visual inspection area, external vial washing and freeze dryer technical area activities. Roles and Responsibilities To ensure cGMP compliance in the department. To ensure area, equipment and line clearance and cleaning of equipment before startup of the operation. To ensure that after completion of operation line closure activity should be performed in accordance with SOPs. To ensure that deviation, change control, CAPA is generated as and when required. To maintain the area cleanliness and arrangement before and after completion of activities. To provide technical support relating to equipment utilized in the area by repairing, maintaining and modifying production equipment utilizing technical expertise, technical manuals, precision tools and test equipment. To provide the versatility training and development of the team members. To prepare the SOPs related to area and contribute to revision of SOPs. To prepare MPCR and to ensure the production operations are followed as per the MPCR. Responsible for completion of all documentation in a timely manner and to ensure that all the

Role & responsibilities Lead formulation and development projects from concept through commercialization Design and optimize formulations to meet product specifications and regulatory requirements Manage and mentor a team of formulation scientists and technicians Collaborate with cross-functional teams including QA, QC, regulatory, and manufacturing Ensure timely completion of project milestones and deliverables Prepare technical reports, presentations, and documentation Stay updated on industry trends, regulatory changes, and best practices Qualifications Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field Minimum of 2-3 years of experience in formulation and development Proven track record of successful product formulations Strong understanding of regulatory requirements and guidelines Excellent project management and leadership skills Strong analytical and problem-solving abilities Fluent English International Travelling - Targeted Country - Ghana, Africa, Nigeria, Ethiopia, Uganda, Kenya, Myanmar, Thailand etc. Skills Formulation development Project management Analytical techniques Regulatory compliance Team leadership Technical writing Problem-solving Benefits Yearly Bonus Provide PF, ESIC, PT Benefits Medical Insurance Travelling Allowances Yearly Increment

Role & responsibilities Role - Aseptic Area Manufacturing Skill operation and supervising of filling machine, sealing machine , ALUS operation , storage vessel operation and cleaning Qualification B. Pharm/M. Pharm Category – Staff

Role & responsibilities For operator Role - Aseptic Area Manufacturing Skill - operation of filling machine (vial or sealing machine) , ALUS operation , storage vessel operation and cleaning Qualification Diploma Eng/ITI

Excellent scope for both (Fresher & Experienced Dermatologist) to offer client consultation, supervise and execute advanced skin & hair cosmetic procedures at the clinic. Responsibilities & Duties: Consult with and treat patients at the designated clinic, perform all dermatology-led medical procedures, and supervise non-dermatology-led procedures. Ensure the efficacy, safety, and adherence to high professional standards for all medical procedures performed under your supervision. Deliver treatments of the highest quality, following established SOPs and company guidelines. Strive for high client satisfaction in all consultations and treatments, as reflected by client feedback and evaluations from the Area Medical Head (AMH) and Area Operations Manager (AOM). Required Candidate profile: MBBS and Masters (MDDVL), Diploma (DDVL, DVD) or Doctorate (DNB) in Dermatology. Strong knowledge and experience in medicine and dermatology. Excellent communication skills and Energy Levels. Ability to connect well with clients. For more details contact 9908974287 or amulya.doni@olivaclinic.com

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 02.08.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. Preparation and review of departmental SOPs 7. Reviewing of Equipment qualification protocols and Reports. 8. Review of supplier qualification documents. 9. Review of calibration documents 10. Receiving and reviewing of executed raw datas & ATRs and archiving for bio batches. 11. Reviewing of analytical method validation protocols & reports. 12. Maintenance, Retrieval and Archiving of all GMP related documents and records. 13. Preparation & review of department Schedules 14. Responsible for document distribution to the user departments. 15. Responsible for Document control activities. 16. Responsible for preparation, review and submitting License Applications. 17. Handling of Change controls (Permanent and Temporary), OOS and Incidents. 18. Responsible for approval of documents in absence of Head FDQA. 19. Responsible for performing job assigned by Head FDQA or his authorized designee. Note : Formulation R&D Candidates also eligible Position : Executive / Senior Executive Qualification : M Pharma / B Pharma Only. Work Location : MSN R&D Center, Pashamylaram. Department : Development Quality Assurance - Formulation Department. Experience : 2 to 8 Years Date of Interview : 02.08.2025 (Saturday ) Interview Time : 9.00 AM to 3.00 PM Venue Details : MSN Laboratories Pvt Ltd. MSN R&D center, Pashamylaram , Isnapur, Patancheru, Sangareddy - 040-30438786

Maintenance Manager Location- Baddi Experience- 12-15 years Salary Package- 9-12 LPA Qualification- B.tech Should have worked in Injectable Unit Must have handled International audits

Hiring for DRA Manager Location- Panchkula Experience- 15+ years Salary Package- 13-17 LPA Must have experience in regulatory Countries dossier preparation and working Should have worked in Injectable Unit Interested One share resume 9815675900

Hiring for f&D Location- Baddi Experience- 4-7 years Salary Range- 40-50 k Industry - Pharma (injectable) interested candidates share resume on 9815675900

Titlle : Manager 1 Engineering Educational Qualification : B Tech/BE Electrical/ Electronics & Instrumentation Engineering Experience: 14 years & above Requirement : 1. To ensure prompt attention and resolve issues of all operational and breakdown maintenance activities related to Utilities, HVAC System, and Water System. 2. To ensure timely execution of Preventive Maintenance of Utilities, HVAC System, Water System & Process Machineries performed as per the SAP schedule and maintain accurate record of the same. 3. To provide Technical assistance & Support for efficient operation of ETP. 4. Review and approve QMS related activities in EDMS & Trackwise systems to ensure compliance and documentation Integrity. 5. Responsible for Compliance of Internal & External Audits. 6. Tracking WBS code for all, CAPEX, Projects & Aspire Projects 7. Conduct Monthly review of MTTR, MTBF & KPIs 8. Following up with OEM, third Party service s & AMC to ensure timely service delivery and issue resolution. 9. Maintaining and ensuring Safety and discipline for all engineering related work and personnel of Engineering. 10. To provide Training to Subordinates to enhance their operational efficiency. 11. To performed any other duties assigned by HOD.

Role & responsibilities Lead Generation & Prospecting: Identify and qualify new business opportunities with pharmaceutical, biotech, and life sciences companies requiring CDMO services. Client Relationship Management: Build and nurture strong, long-term relationships with prospective and existing clients to understand their development and manufacturing needs. Proposal Development: Collaborate with internal technical, project management, and finance teams to develop proposals, quotes, and presentations tailored to client requirements. Contract Negotiation: Lead contract discussions, ensuring alignment between client expectations and company capabilities while maintaining profitability. Market Intelligence: Monitor industry trends, competitive landscape, and customer needs to refine BD strategy and identify growth areas. Sales Forecasting & Reporting: Maintain an accurate sales pipeline, forecast revenue, and report performance metrics to senior leadership. Cross-Functional Collaboration: Work closely with R&D, operations, regulatory, and quality teams to ensure successful onboarding and execution of new projects. Event Participation: Represent the company at trade shows, conferences, and networking events to build visibility and generate leads. Preferred candidate profile Experience of working in 3 to 5 years in US Market Strong expertise in sterile pharmaceutical manufacturing, with 35 years of relevant experience. Bachelors degree in Pharmaceuticals (Masters or MBA preferred). 5+ years of experience in business development, sales, or account management within a CDMO, CMO. Strong understanding of the pharmaceutical product lifecycle, from preclinical development through commercial manufacturing. Proven track record of meeting or exceeding sales targets. Excellent communication, negotiation, and presentation skills. Ability to work independently in a fast-paced, dynamic environment.

Responsible for leading production operations, coordinating production staff and equipment, ensuring product quality and profitability, and overseeing and managing the production operations involved in injectable products.

Company Description Orchid Pharma is a well-established and reputed company, listed on the stock exchange that has now re-entered the formulations business in India, with an initial focus on hospital segment. Orchid is the only Indian company to get USFDA approve manufacturing plant for Cephalosporins. We have launched the critical care division with focus on Injectable Antibiotics & Antifungals. Role Description Position Title: Hospital Sales Executive Reports To: Key Account Manager, Orchid Pharma Formulations Division Responsibilities Achievement of sales targets for the assigned Key Accounts (Monthly, Quarterly and Annually) both in Primary & Secondary, with tight control on commercial policy discipline. Drive the Sales Plan based on:a) Deep understanding of each Key Account, in terms of their systems and processes, Key decision makers and influencers, antibiotic consumption patterns. b) Analysis of market trends & competitor activitiesc) Analysis of our own sales (SKU wise), volumes and net prices / discounts Building direct and personal relationships with key decision makers in key customers eg KOLs, HODs, CIP (Commercially Important Person) etc under the guidance of KAM. Promoting products in specialized therapeutic area under the guidance of KAM. Liaise with and persuade targeted doctors to prescribe our products utilizing effective selling skills. Promote products ethically and within compliance based on company's sales process and approved marketing strategy Skills and Competencies Results Orientation and Action Orientation Planning and Analytical ability Persuasive Influencing skills, High Relationship Skills and engage internal stakeholders effectively Technical Skills Strong understanding of pharmaceutical use in hospitals, especially Antimicrobials / Critical Care Proven expertise in Hospital sales with good understanding of their purchase decision making process Proficient with MS office and other online reporting tools Profile & Education Bachelor in Science / B. Pharma or relevant field Experience Minimum of 1 to 5 years of experience in sales management, product management / key account management with a proven record of accomplishment of achieving sales targets. B Pharma Freshers can also apply Industry Pharmaceutical (preferably from Critical Care / Antimicrobials) Age: Up to 35

Educational Requirements Bachelor of Engineering Service Line Infosys Quality Engineering Responsibilities Global Pay Plus Testers. MT MX messaging , SWIFT payments Preferred Skills: Banking-GPP Financial Services Domain-Payments-GPP Generic Skills: Banking

Good knowledge of cGMP, documentation practices, and regulatory requirements. Experience with visual inspection, labeling, sealing, and secondary packaging.

Prototype formulation design to Lab scale development, process optimization using DOE, Characterization of complex formulations by advanced techniques, and Interpretation of data, handling of regulatory queries, and preparation of justifications.

Job Title: Production Manager Department: Production Production Manager Injectables with full manufacturing knowledge including formulation, filling, sterilization, and packaging. Strong technical knowledge of sterile/injectable manufacturing. Supervise and manage day-to-day production activities for injectable formulations. Prepare and review production plans, BMRs, SOPs, and validation protocols. Key Responsibilities: Formulation / Compounding Filling & Sealing Sterilization Visual Inspection Packaging Team Management & Training

The candidate will be responsible for the proper receipt, storage, and GMP-compliant dispensing of raw materials used in pharmaceutical production Perform raw material dispensing activity in designated dispensing booths under controlled conditions.. Required Candidate profile Receive, inspect & label incoming raw materials as per SOP Coordinate with the QA, Production & QC department during material movement Ensure adherence to GMP, GDP & safety guideline during dispensing

* Implement and manage production processes for injectable DPI and liquid injection product. * Ensure all operations comply with GMP and regulatory requirements. * Prepare daily reports and update process documentation consistently Required Candidate profile * Knowledge of Peptide synthesis, Purification & Lyophilization operation. * Operation of reactor, Nutsche filter, centrifuge * Handling experience of equipment Lyophilizer and Autoclave

Carry out literature search for upcoming products and accordingly plan for product development. Preparation of product feasibility report. Knowledge in the formulation development of Parenteral dosage forms. Development flow for Parenteral dosage form. Guidance to fellow colleagues regarding development flow. Hands on experience in Formulation Development including pre-formulation study and Scale-up. Initiation of Filter validation study with filter supplier. To prepare Product development report (PDR). Good hand at Compatibility studies for Finish product. Visualize developmental needs of the product (i.e. API, Excipients, Packing materials). Solve the problems and quires related to the development of the formulation and discuss with team members. Transferring of new developed product to the Manufacturing site. Understand/Familiarize with the problems faced during scale-up batches, trouble shooting. Compilation and interpretation of routine analytical data. Preparation of SOPS, MFR, Stability & Hold Time studies protocol, writing of Lab notebooks. Preparation of in-process finished product specification and packing material specifications consulting with ADL personnel. Have Sufficient Knowledge of regulatory guidelines (EU, ROW and US Markets). To provide technical support for commercial batch manufactured. To perform investigation of failures during exhibit batches/stability study. Supporting role for OSD development including literature, documentation, and trial batches at FRD.

Multiple Positions open for Officer/Manager Role & responsibilities : Managing the production line with end to end responsibility for Quality and Quantity. Also required to complete requisite documentation and MIS as desired by management. Preferred candidate profile: S cience Graduate with 3-11 years of experience in managing Filling Lines/Batch Manufacturing/Packing operations in the pharmaceutical industry. Preference will be given to candidates with Injectable operations experience. Should be able to handle 6-10 supervisors Perks and benefits : Best in Industry salaries, growth opportunities within the organization and a fair minded organization which respects individuals as contributors.

Role & responsibilities Handling of pre and post approval regulatory activities of US/EU/CA submissions. Review of developmental documents for regulatory submission. Good knowledge of handling CMC documentation for Dossier submission Compilation and Submission of Annual reports and Supplements. Having the experience of solid orals and injectables. Preparation of Sterility Assurance Package for injectable Dossiers. Preparation of Pre-IND/scientific advice meeting packages Drafting, compiling & eCTD publishing of dossiers for regulatory filings. Review of specifications and test procedure as per pharmacopoeia requirements. Providing regulatory support for customer filings and customer queries. Evaluation of regulatory authority deficiencies and preparation of action plan accordingly. Also follow up of response documents with concern stake holders. Evaluation and approval of QMS documents, wherever applicable. To update cross functional teams for different regulatory compliance & requirements. Responsible for outlining requirements for labelling, storage and packaging. Review of product development report and QBD concepts. Updating product approval package to plant team. Preferred candidate profile Should Have Formulation Regulatory Affairs Relevant Experience in US/EU/Canada Perks and benefits

Experience Required :- Must have exp of Hospital Sales Must have exp of Critical Care Division OR Surgical Sales If interested pl. share your cv on talentacquisition.delhi1@romsons.com pl. contact on 9643975459