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As the Quality Control Officer, you will be responsible for ensuring the overall quality of products and compliance with GMP at the site. This includes conducting line clearance prior to dispensing, manufacturing, packing, and validation activities. You will also be involved in sampling during the manufacturing of validation, exhibit, and commercial batches, as well as in-process control, routine inspection, and online process verification and documentation. Your duties will involve the preparation, review, and approval of various documents such as SOPs, BMRs, BPRs, SMFs, VMPs, APQRs, MFR validation protocols/reports, and qualification protocols/reports. Additionally, you will be responsible for executing and evaluating qualification and validation studies, as well as evaluating and authorizing rework or reprocessing of batches. Your role will also include reviewing batch documentation and releasing batches for distribution, and ensuring quality control functions to maintain GLP and data authenticity. Furthermore, you will review and approve worksheets, COAs, raw and packing material specifications, semi-finished specifications, finished product specifications, and stability protocols. You will also review stability data generated at the site and submit it to Regulatory Affairs for dossier preparation. Additionally, you will be tasked with controlling, distributing, retrieving, and destroying master and executed documents such as BMRs, BPRs, analytical workbooks, master SOPs, protocols, reports, and logbooks. Qualifications required for this role include a Bachelor's degree in Pharmacy or Chemistry, knowledge of cGMP, and a minimum of 3 years of experience in the Pharmaceutical industry. This is a full-time position with benefits such as food provided, health insurance, life insurance, paid sick time, and Provident Fund. The work schedule involves rotational shifts, and there is a yearly bonus offered. The work location is in person, and the application deadline is 20/06/2025, with an expected start date of 20/08/2025.,

Job description The incumbent should be aware of the product development flow from the conceptualization to tech transfer The incumbent is responsible for R&D trials batch making for various personal care / personal hygiene products like Creams / Lotions Suspensions Shampoos/ Face washes Face Powders etc. Would be responsible for performing pre-stability for the developmental products Need to be actively involved in discussion with internal & external stakeholders. To be involved for handling Tech Transfers of products to the manufacturing sites as & when required.

Job description The incumbent should be aware of the product development flow from the conceptualization to tech transfer The incumbent is responsible for R&D trials batch making for various personal care / personal hygiene products like Creams / Lotions Suspensions Shampoos/ Face washes Face Powders etc. Would be responsible for performing pre-stability for the developmental products Need to be actively involved in discussion with internal & external stakeholders. To be involved for handling Tech Transfers of products to the manufacturing sites as & when required.

Key Responsibilities Conduct Pilates Classes: Lead group and private Pilates sessions, ensuring exercises are performed correctly and safely. Develop Personalized Programs: Design customized Pilates routines tailored to individual client needs and fitness levels. Qureos Monitor Client Progress: Assess and track clients' physical progress, adjusting programs as necessary to meet their goals. CareerExplorer Ensure Safety Standards: Maintain a safe exercise environment by inspecting equipment and ensuring proper use. Club Pilates West Palmdale Provide Instruction and Feedback: Offer clear demonstrations and constructive feedback to clients to improve performance and prevent injury. CareerExplorer Stay Updated: Continuously update knowledge of Pilates techniques and trends to provide the best instruction.

Visiting to DS manufacturing and warehouse facility to ensure that activities are being carried out by following GMP requirements, Regulatory requirement and as per approved procedures. Line clearance for the process operation during manufacturing activity (Drug Substance). Preparation and review the Risk Assessment and Mitigation Plan. Ensure that process and cleaning validation activities are being carried out by following approved protocols. Review of master document like study protocol, BPR, MFR etc Review of executed Batch Processing Records for Batch Release. Review of Batch Dispatch Record and verification of dispatch activities in warehouse. Preparation and review of Quality System SOPs documents. Review of SOPs as per GMP requirements for all departments. Education Masters in Biotechnology or Biotechnology Competencies 1. Strategic Agility 2. Innovation Creativity 3. Customer Centricity

Filling & review BMRs, MFRs, SOPs, ECR Maintain records for CC, CCF Ensure documentation aligns with GMP Requirement Support audits & investigations with accurate records. Coordinate with production & QA for data verification. Required Candidate profile Must Require Knowledge for filling & Review of BMR BMR, CC, CCF, and OOS handling Documentation practices & regulatory understanding Good communication & MS Office proficiency

Job Purpose Key Result Areas Supporting Actions Accountability: Safety Implementation : Organize and coordinate safety practices in the plant to achieve zero Accident target. 1. Plant Inspections. 2. Develop Checklist. 3. Monitor and implementation. 4. Participation in departmental meetings. 5. Emphasis on usage of PPE. 6. Generate and review of reports and analysis of accident. 7. Conducting training program Safety Promotion: Identify and formulate programs related to safety in order to motivate the employees. 1. Suggestion scheme. 2. Award and recognition. 3. Display boards, posters / slogans. 4. Safety pledge every month involving all employees. 5. Awareness campaign. Development of safety procedures: Investigation and analyzing accidents to develop standard practices of safety. 1. Identify hazards. 2. Counter measure of hazards. 3. Audit of practice. 4. Interactive suggestions. 5. Cause of accidents & Type of injury. 6. Causation model. 7. Identify areas of unsafe conditions. 8. Recommending action plan. Statutory Compliance: To Monitor and compliance of statutory requirements pertaining to safety rules and regulations. 1. Organize safety committee meetings. 2. Organize reports to accident and send to personnel department. 3. Compliances as per factories Act 1948 / MFR 1963. 4. Safety auditees / inspections / load or pressure tests as per legal requirement. Safety Implementation: Organize & coordinate with Section Heads and monitor implementation of safety practices in the Unit to achieve zero Accident target. 1. Guide for effective implementation of Safety culture. 2. Impart training to workmen/contract workmen. 3. Identification & rectification of unsafe points/defects 4. Regular checking of process safety interlocks. 5. Regular checking of tools & tackles. 6. Analyze accident/near miss cases and SBO. 7. Carryout safety/environment audits as per corporate safety requirements. 8. Monitor working of pollution control equipment 9. Conduct Tool box meetings/talks. 10. Adherence to LOTOTO, CSM, PTW, JCC as per corporate requirement. 11. Reporting NMC, involvement in CFSA and SBO. 12. Insist all employees and workman for following safety systems/safe practices at the Unit Implementation of WCM system. 1. Review of WCM practices, Ensure daily 5S activities, timely rectification of abnormalities. 2. Coordinate for painting of Visuals and Posters for Safety and WCM. 3. WCM system training and Model area development 4. Organizing Mega Cleaning. 5. Ensure KFA Team meetings with updation of activity boards. 6. Involvement in audit. 7. Model Area assessments, WCM assessments. 8. Identifying abnormality during Mega cleaning activity. Safety Management System Updating and sustaining with ISO 45001:2018 system by documents management, Internal Audits, Coordinating External Audits. People Management Enhancing skill of people through continuous learning and assigning projects.

Role & responsibilities Responsibility of Downstream activities in bulk manufacturing facility. To ensure that Downstream batches are carried out as per manufacturing instructions following relevant Process Development description document, MFR, SOPs, BPRs, Protocols etc. and to ensure appropriate documentation in order to maintain cGMP compliance. Preferred candidate profile To understand and follow the safety practices and usage of PPEs in Bulk manufacturing facility and during process. Execution of Scale up of Development batches in Bulk manufacturing facility. Tracking of inventory of consumables used in manufacturing. Ensure Facility monitoring, readiness & maintenance of BM facility. Coordination with Engineering department on tracking and completion of preventive maintenance of Downstream Equipments and instruments. Following good documentation practices such as online documentation like BPR, equipment log, record sheets, etc. in Downstream process. Preparation of Batch production records, SOPs, record sheets and related documents for Downstream related activities in Bulk Manufacturing Facility. Review of Batch production records and related documents in Downstream process. Responsible for timely closure of Batch production records (BPRs), Protocols and reports related to the Downstream process. Coordination with Vendors on equipment and instruments qualification related to the Downstream process. Initiation and closure of change controls, deviations related to Bulk Manufacturing area. Ensure the timely revision of BPR, SOP and study protocols related to downstream process. Responsible for LMS activities as a department training coordinator. Involving in internal audits, local DCGI audits and any other regulatory agencies. Involving in training on safety related activities and imparted training to pooled staff.

Preparation of CTD(Common Technical Documents) and ACTD(Asian Common Technical Documents) Dossiers for CIS (Commonwealth Independent States) and ROW (Rest Of World) Reviewing factory documents like Specifications, MOA (Mode Of Action), COA (Certificate Of Analysis), BMR (Batch Manufacturing Records), PVP (Polyvinylpyrrolidone), PVR (Pharmaco Vigilance Regulation), MFR (Master Formula Records), Stability Data etc.Reviewing DMF (Drug Master File) Reviewing Artworks and Labels. Co-ordinating with Factory for Documents. Preparation of Normative Document of Registered productsin CIS markets.Preparation of Excel sheet of Regulatory status. Response to Queries. Filing of Documents / Dossier. Preparation of DMF. Co-ordinating with respective person for Tender Documents. Filing of NDA (New Drug Application) & MAA (Marketing Authorisation Application). Other Regulatory / Compliances related responsibilities. Liaisoning with National & International Authorities for Regulatory related work. Candidate Profile: Presently working in similiar capacity i.e. as Export Executive/Manager with any leading Pharma Company. Candidate must be a Graduate/D.Pharm/B.Pharm or MBA preferably in Regulatory Affairs. 2 - 5+ years Andheri (E),Mumbai Local Resident of Mumbai preferred Male / Female Candidate Only Only those candidates who have worked in Pharma Industry in this profile.

Role & responsibilities: Preferred candidate profile :

Female B.Pharm / M.Pharm with 4 to 6 years of experience in Regulatory Affairs. Dossier Preparation in CTD/ACTD/Country Specific Formats. Re-registration and Renewal Application. Variation Application, Queries Handling, DMF Activity & Artwork Review. Required Candidate profile Country Experience Required: Uzbekistan, Kazakhstan, Azerbaijan, Turkmenistan & Tajikistan Dosage Form Experience Required: Tablets, Capsules, Oral Powder, Gel & Cream, Injections, Syrup, Oral Drops Perks and benefits Negotiable - Depending Upon Candidate & Experience

Female B.Pharm / M.Pharm with 4 to 6 years of experience in Regulatory Affairs. Dossier Preparation in CTD/ACTD/Country Specific Formats. Re-registration and Renewal Application. Variation Application, Queries Handling, DMF Activity & Artwork Review. Required Candidate profile Country Experience Required: Uzbekistan, Kazakhstan, Azerbaijan, Turkmenistan & Tajikistan Dosage Form Experience Required: Tablets, Capsules, Oral Powder, Gel & Cream, Injections, Syrup, Oral Drops Perks and benefits Negotiable - Depending Upon Candidate & Experience

Female B.Pharm / M.Pharm with 4 to 6 years of experience in Regulatory Affairs. Dossier Preparation in CTD/ACTD/Country Specific Formats. Re-registration and Renewal Application. Variation Application, Queries Handling, DMF Activity & Artwork Review. Required Candidate profile Country Experience Required: Uzbekistan, Kazakhstan, Azerbaijan, Turkmenistan & Tajikistan Dosage Form Experience Required: Tablets, Capsules, Oral Powder, Gel & Cream, Injections, Syrup, Oral Drops Perks and benefits Negotiable - Depending Upon Candidate & Experience

Female B.Pharm / M.Pharm with 4 to 6 years of experience in Regulatory Affairs. Dossier Preparation in CTD/ACTD/Country Specific Formats. Re-registration and Renewal Application. Variation Application, Queries Handling, DMF Activity & Artwork Review. Required Candidate profile Country Experience Required: Uzbekistan, Kazakhstan, Azerbaijan, Turkmenistan & Tajikistan Dosage Form Experience Required: Tablets, Capsules, Oral Powder, Gel & Cream, Injections, Syrup, Oral Drops Perks and benefits Negotiable - Depending Upon Candidate & Experience

Female B.Pharm / M.Pharm with 4 to 6 years of experience in Regulatory Affairs. Dossier Preparation in CTD/ACTD/Country Specific Formats. Re-registration and Renewal Application. Variation Application, Queries Handling, DMF Activity & Artwork Review. Required Candidate profile Country Experience Required: Uzbekistan, Kazakhstan, Azerbaijan, Turkmenistan & Tajikistan Dosage Form Experience Required: Tablets, Capsules, Oral Powder, Gel & Cream, Injections, Syrup, Oral Drops Perks and benefits Negotiable - Depending Upon Candidate & Experience

Female B.Pharm / M.Pharm with 4 to 6 years of experience in Regulatory Affairs. Dossier Preparation in CTD/ACTD/Country Specific Formats. Re-registration and Renewal Application. Variation Application, Queries Handling, DMF Activity & Artwork Review. Required Candidate profile Country Experience Required: Uzbekistan, Kazakhstan, Azerbaijan, Turkmenistan & Tajikistan Dosage Form Experience Required: Tablets, Capsules, Oral Powder, Gel & Cream, Injections, Syrup, Oral Drops Perks and benefits Negotiable - Depending Upon Candidate & Experience

Plan, setup, monitor, and workup chemical reactions independently Monitor progress of the reactions by using standard methods and analytical techniques (TLC, GC, HPLC, LCMS etc) Isolate product and Optimize reaction conditions for improved yields and output Purify compounds by different methods using chromatography, distillation and crystallization etc. Characterization and identification of compounds using UV, IR, NMR, LCMS and GCMS etc Ensure parallel execution of multiple reactions conducted both by self and the team Scale up of R&D developed products to kg scale and then technology transfer to pilot plant Troubleshoot as appropriate for successful execution with intimation to supervisorautomation Writing regular updates, final reports, PDR preparations and inter departmental communication

Responsibilities • Strong assessment & diagnostic skills • Experience in dry needling & cupping • 2+ yrs experience in a clinical setup • Exp. in manual therapy, manipulations & musculoskeletal conditions • Treated patients of all age groups & genders

Preparation of MFR, BMR and BPR. Preparation of batch manufacturing records, Batch packing record of all dosage forms.

Role & responsibilities Responsibility of Upstream activities in bulk manufacturing facility. To ensure that upstream batches are carried out as per manufacturing instructions following relevant Process Development description document, MFR, SOPs, BMRs, Protocols etc. and to ensure appropriate documentation in order to maintain cGMP compliance Preferred candidate profile Preparation of process documents (PCS, MFR, BMR), SOPs, protocols, related documents for upstream activity. Hands on experience in operations of seed and production fermenters, continuous centrifuge, homogenizer and continuous involvement and support for commercial batches etc., Involving and supporting in Sun Pharma CQA audits, internal audits ,local DGCI audits CDSCO and any other third party/national &international regulatory agencies. Review of batch manufacturing records and related documents in upstream. To understand and follow the safety practices and usage of PPEs in Bulk Manufacturing facility and during process. Execution of Scale up of Development batches, commercial batches and other assigned tasks in Bulk manufacturing facility as per the assigned shift schedule (A,B,C Shift) hours. Ensure Facility monitoring, readiness & maintenance of BM facility. Coordination with engineering department on tracking and completion of preventive maintenance and calibration of Upstream process Equipment and instruments. Following good documentation practices such as online documentation like BMR, equipment log, record sheets, etc. in upstream process. Following up with Vendors on equipment and instrument related to upstream process. Support for creation of Process Order/material reservation related to SAP transactions and handling of QMS elements activities. Support and fulfill for any additional job work activities /other job responsibilities/tasks assigning by reporting manager.

Role & responsibilities Inspection - release/rejection of incoming material against approved specification. Rejection of material non conformance review, reporting in IMSxpress. Updation of critical incoming material list (incoming material specification) based. Allocation of catalogue number to finished products depending on customization/changes in product. Control of documents (QSP, SOP, formats, MFR, MQR) issuance, retrival, archival and updation in IMSxpress. Compiling of data for MIS as per schedule Allocation of batches as per customer purchase order over mail. Review of certificate of analysis for finished products. Daily IPQA of production and BMF as per the approved protocols and procedures and subsequent reporting. Issuance and handling of change control, non conformity, CAPA in IMSxpress Issuance and handling of Deviations Issuance and maintenance of BMR Handling, Recording and compilation of customer complaints Updation and maintenance of departmental risk register. Participating in product Validation. Review of packing order, checking of labels and Shipments to customers. Participating in Internal/external audit as per audit agenda and responsibility allotted. Preferred candidate profile Should have a Bachelors or Master's degree in pharmacy/biotechnology/Biochemistry or other relevant scientific discipline with 2/3 years experience in Quality Assurance. Knowledge of GMP standards, SOPs and quality management systems • Awareness of QMS as per ISO13485: 2016 and ISO 9001:2015 standards • Data collection and management • Customer service orientation • Excellent relationship management skills with the ability to engage, negotiate and manage key stakeholders and suppliers • Strong and confident negotiator with the ability to negotiate at all levels • Excellent communication, interpersonal and influencing skills • Results orientated with ability to plan and deliver against deadlines • Ability to add value, reduce costs and make improvements • Computer literate, especially Excel skills

Roles and Responsibilities Develop new products by formulating, developing, and launching solid oral products. Conduct bioanalytical testing to ensure product quality and stability. Collaborate with cross-functional teams for process development, PDR (Process Development Research), MFR (Manufacturing Formulation Research), FD Trial (First Time Right Trial). Ensure compliance with regulatory requirements through documentation of SOPs, BPRs, and batch records. Provide technical support to production team on product-related issues.

Analyst/ Senior Analyst -Bankruptcy Specialist Number of positions to be closed : 5 Work Model : Work From Office Only Flexible to work in Night Shifts (US Timings) Experience :- 2+Years Preferred :- Only Immediate Joiner Location:- Mahadevapura, Bengaluru Interested candidates can connect immediately by calling or WhatsApp at 7892648654 to schedule the interview. Job Overview: Strong knowledge about Bankruptcy Reconciliation process and the Bankruptcy support services Good understanding towards review of statements, calculations and tasks related to Reconciliation Strong Knowledge towards Ledger preparation, Proof of Claim and Motion for Relief, PPFN, PCN processes. Reviewing of all the required Foreclosure documents for the relevant Bankruptcy task. Also, should have basic knowledge of all the processes under Bankruptcy. Reviewing the borrower details to determine whether the borrower is falling under any state regulated protections which in turn will influence Bankruptcy Good knowledge of reviewing Mortgage and Bankruptcy related documents Ensure all assigned cases are worked in accordance with regulatory, investor/insurer, and Trust Policy requirements and timelines. Update and document all tracking systems including the clear and accurate documentation of the accounts worked Roles & Responsibilities Processing tasks as per the process guidelines Meeting assigned productivity and quality targets Adhering to SLAs and TATs Candidate should be open to work in shifts. Interpersonal relationship at work with peers Adhering to organization policies Qualification & Experience Educational qualification and years of experience required in any specific domain/skill for the role Basic Degree completion (15 years of education) Good written and oral communications skills in English US Mortgage Experience in Bankruptcy Reconciliation and related process and (Minimum 12 Months experience) Hands-on experience in handling • Payment Ledgers and Manual Payment History Creation (especially for POC/MFR) • Bankruptcy Closings • 410A Forms • Proof of Claims (POCs) • Reaffirmation Agreements • Post-petition and Pre-petition payment calculations • Complete working knowledge of Chapter 13 and Chapter 7 The candidate should have descent communication Shift timings:- 5.30 PM to 2.30 AM or 6.30 PM to 3.30AM Only one way transport will be provided for drop in the night after 10.00 PM with the radius of 25kms. Mandatory Note : Required on education with 10th ,12th and Degree Marksheets and Certificates and there previous and current company Offer Letters and Relieving Letters along with current company 3-month pays slips which are mandatory Documents.

Greetings from Adecco..!! Hiring for Bankruptcy Job Location- Bangalore Salary- up to 5 LPA Share CV mohini.sharma@adecco.com OR WhatsApp on (9740521948) Periodic review of the loans in Bankruptcy portfolio and provide direction to cash team on how to post funds received. Monitor the transactions posted on Bankruptcy accounts for accuracy and compliance. Verify posting/receipt of funds against Trustee websites. Respond to customer complaints/inquiries. Manage processing & payment of vendor invoices through system or manual check requests Ensure all assigned cases are worked in accordance with regulatory, investor/insurer, and Trust Policy requirements and timelines. Update and document all tracking systems including the clear and accurate documentation of the accounts worked Roles & Responsibilities Processing tasks as per the process guidelines Meeting assigned productivity and quality targets Adhering to SLAs and TATs Candidate should be open to work in shifts. Interpersonal relationship at work with peers Adhering to organization policies

Analyst/ Senior Analyst -Bankruptcy Specialist Number of positions to be closed : 5 Work Model : Work From Office Only Flexible to work in Night Shifts (US Timings) Experience :- 2+Years Preferred :- Only Immediate Joiner Location:- Mahadevapura, Bengaluru Job Overview: Strong knowledge about Bankruptcy Reconciliation process and the Bankruptcy support services Good understanding towards review of statements, calculations and tasks related to Reconciliation Strong Knowledge towards Ledger preparation, Proof of Claim and Motion for Relief, PPFN, PCN processes. Reviewing of all the required Foreclosure documents for the relevant Bankruptcy task. Also, should have basic knowledge of all the processes under Bankruptcy. Reviewing the borrower details to determine whether the borrower is falling under any state regulated protections which in turn will influence Bankruptcy Good knowledge of reviewing Mortgage and Bankruptcy related documents Ensure all assigned cases are worked in accordance with regulatory, investor/insurer, and Trust Policy requirements and timelines. Update and document all tracking systems including the clear and accurate documentation of the accounts worked Roles & Responsibilities Processing tasks as per the process guidelines Meeting assigned productivity and quality targets Adhering to SLAs and TATs Candidate should be open to work in shifts. Interpersonal relationship at work with peers Adhering to organization policies Qualification & Experience Educational qualification and years of experience required in any specific domain/skill for the role Basic Degree completion (15 years of education) Good written and oral communications skills in English US Mortgage Experience in Bankruptcy Reconciliation and related process and (Minimum 12 Months experience) Hands-on experience in handling • Payment Ledgers and Manual Payment History Creation (especially for POC/MFR) • Bankruptcy Closings • 410A Forms • Proof of Claims (POCs) • Reaffirmation Agreements • Post-petition and Pre-petition payment calculations • Complete working knowledge of Chapter 13 and Chapter 7 The candidate should have descent communication Shift timings:- 5.30 PM to 2.30 AM or 6.30 PM to 3.30AM Only one way transport will be provided for drop in the night after 10.00 PM with the radius of 25kms. Mandatory Note : Required on education with 10th ,12th and Degree Marksheets and Certificates and there previous and current company Offer Letters and Relieving Letters along with current company 3-month pays slips which are mandatory Documents. Interested candidates can connect immediately by calling 9686640353 to schedule the interview. Vijaya Durga gentella.vijayadurga@adecco.com