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Analyst/ Senior Analyst -Bankruptcy Specialist/End to End Foreclosure Specialist Work Model : Work From Office Only Flexible to work in Night Shifts (US Timings) Experience :- 2+Years Preferred :- Only Immediate Joiners F2F Interview Location:- Bengaluru Share updated resume - Gentella.VijayaDurga@adecco.com whatsapp at -9686640353 1-BANKRUPTCY- 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 2- FORECL...

Analyst/ Senior Analyst -Bankruptcy Specialist/End to End Foreclosure Specialist Work Model : Work From Office Only Flexible to work in Night Shifts (US Timings) Experience :- 2+Years Preferred :- Only Immediate Joiners F2F Interview Location:- Bengaluru Share updated resume at siddhi.pandey@adecco.com or whatsapp at 6366783349 1-BANKRUPTCY- 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 2- FORECLOSUR...

Job Summary: The Bankruptcy Consultant provides expert advice and support to clients or the organization in matters related to insolvency, bankruptcy, and corporate restructuring. This role involves analyzing financial statements, evaluating debt structures, guiding legal proceedings, and recommending strategies for debt resolution or business recovery. The ideal candidate should have strong financial, legal, and analytical skills , along with knowledge of bankruptcy laws and regulatory frameworks. Key Responsibilities: Client Advisory & Consultation Advise clients on bankruptcy, insolvency, and debt restructuring options. Conduct detailed financial analysis of distressed companies or indivi...

About the Role: We are seeking an experienced and detail-oriented Bankruptcy Specialist to manage and process bankruptcy cases involving client accounts, ensuring compliance with legal and regulatory requirements. The Bankruptcy Specialist will serve as the primary liaison between internal departments, external legal counsel, and courts, while supporting efforts to protect the organizations financial interests. Key Responsibilities: Bankruptcy Case Management Review, process, and monitor bankruptcy filings, claims, and court documents . Manage and maintain accurate records of all bankruptcy cases in internal systems. File proofs of claim, reaffirmation agreements, and other bankruptcy-relate...

In this role at ZRC BIOTECH, you will be responsible for various tasks within different groups as outlined below: **Analytical Group:** - Design, perform, and review HPLC\UPLC, structural, and mass spectrometry based experiments. - Develop, qualify analytical methods, and transfer technology. - Prepare STP, SOP, and TTD documentation. - Perform routine calibration of instruments. - Maintain day-to-day compliance of the laboratory. - Manage samples including procurement of materials required for lab activities. **Formulation Development Group:** - Prepare technology transfer documents and collaborate cross-functionally with different teams. - Develop packaging for late phase batches, clinical...

Manager - Quality Control (Formulations) 10 to 15 years of experience in Pharmaceutical Industry especially in Formulations Unit. Should have experience in successfully handling Quality Audits. Thorough knowledge in all types of Analytical instruments, analytical methods, HPLC, Method validation and method development etc., Should possess profound knowledge and skills in OSD/Formulations products. Total Quality Management (TQM), preparation and successful implementation of SOP's. Should lead a team in QC department and responsible for TQM. Sound working knowledge in MS Office and computer skills. Responsible for day-to-day and periodical MIS reports. Coordination with Production, QA and othe...

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:- 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 Foreclos...

Key Responsibilities: Preparation, review, and control of Master Formula Records (MFRs) and Batch Manufacturing Records (BMRs). Identification, drafting, review, and periodic revision of Standard Operating Procedures (SOPs) across departments. Compilation and preparation of Annual Product Quality Review (APQR) reports. Preparation, review, and execution of Qualification & Validation documents (equipment, utilities, process, cleaning, etc.). IPQC management ensure in-process checks are conducted as per defined procedures and documented appropriately. Ensure timely product release as per defined process and quality requirements. Work on company-wide quality strategies aimed at reducing non-com...

Roles and Responsibilities Develop new products by formulating, processing, and developing solid oral dosage forms such as tablets, capsules, granules, etc. Conduct BMR reviews to ensure compliance with GMP guidelines. Collaborate with cross-functional teams for batch manufacturing of OSDs (Oral Solid Dose) products. Ensure knowledge of RMG (Raw Materials Group) management and Batch Manufacturing Record review. Provide support in production activities related to solid oral dosage forms. Identify areas for improvement in production processes, implement changes to increase efficiency and productivity while maintaining quality. Investigate and resolve production issues, including equipment malf...

Roles: Plant inspections Develop checklist Monitor and implementation Participation in departmental meetings Emphasis on usage of PPE Generate and review of reports and analysis of accident Conducting training programs. Safety Promotion :- Identify and formulate programs related to safety in order to motivate the employees Suggestion scheme Award and recognition Display boards, posters/Slogans Safety pledge ,every month involving all employees Awareness campaign. Development of safety procedures: Investigation and analyzing accident to develops standard practices of safety. Identify Hazards Counter measure of hazards Audit of practice Interactive suggestions Cause of accidents Type of injury...

Credit Management Ensure Timely Block Circulation to Commercial Team Ensure to Credit Block Release as per Credit Policy Enhance to Improve credit block review system and best utilization of resources Driving Collection and reducing overdues by partnering with sales team Improve AR ageing quality & achieve DSO Target through continuous monitoring Credit Limit and Terms review for existing customer in peak period of the year and for New customer by reviewing the assigned quota and as per the average expected share / sales to Diageo India. Debtor Estimates / forecast review basis actual Debtor reports to ensure no Risk in AR. Support RTM Changes / Annual policy changes No sales loss due to sys...

Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace always. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team includi...

Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams. Devising ways to improve the manufacturing process to ensure higher-quality goods. Required Candidate profile Strong attention to detail, observation, organizational, and leadership skills. Knowledge of quality control procedures and legal standards. Good technical and IT skills. Perks and benefits Bonuses Flexible Work Arrangements Paid Time Off

Execution of Project technical feasibility experiments. Initiate Resource procurement Execution of developmental trials, PDR studies/QBD additional studies for ANDA injectable products. Compilation of developmental data Prepare technical documents e.g. MFR, PDR and other protocols reports. Coordination with CFTs (ADL, IRA, Procurement, Quality) for on time resource availability. Successful execution of Exhibit batches at Baxter / CMO sites. Review of commercial products Raw material, packing material product specifications. Perform remediation trials and document preparation based on Regulatory commitments/OOS/Project CCNs/CAPA/Product nature and criticality. Perform trials for regulatory qu...

Position: QA Executive Job Location: Nerul, Navi Mumbai Industry: Ayurvedic / Herbal Pharmaceuticals Qualification: B.Pharm /M. Pharm Designation & Salary: Commensurate with industry experience and expertise. Working Days And Time: 8:00 AM to 5 PM / 6 Days week / Sunday fixed Off. Key Responsibilities: Preparation and implementation of Standard Operating Procedures and Documentation like preparation of MFR, BMR, BPR, all types of Validation, Stability study protocols and reports. To implement and enforce cG.M.P. as per statutory requirements Giving feedback to management regarding discrepancies, deviations and any special matter. To attend external official work, seminars, meetings, discussi...

To perform the manufacturing activities as per the batch processing record, To perform the disinfectant preparation, ensure and perform the area cleaning activities, Responsible for batch calculation and check the dispensed materials. To ensure and perform the CIP, SIP, filter integrity and batch preparation activities. Responsible for the reconciliation of filled and sterilized bottles. To keep all the equipment in working condition and check and monitor the scheduled PMP activities Co-ordinate with other relevant department regarding manufacturing, sampling and other stages of the process as per the batch processing record. Record deviations and discrepancies in the batch stages and report...

We required candidate for the position of AGM-Formulation Exp in OSD-Immediate Release (IR),Extended Release (ER),Powder for Suspension(PFOS) &Oral Liquid dosage forms for US,EU&Canada. T-Exp-15 + CTC-Upto 30.00Lacs Loc-Mumbai(Kandivali)

This position requires individuals to use expertise in areas of development and Support of MFR project independently and in a team. Capably handles multiple tasks and switches from task to task without loss of efficiency. Recommends and makes changes and enhancements to improve the quality of products and procedures. Writes and implements efficient code. Works with team members to conduct root cause analysis of issues, review new and existing code, and perform unit testing. Mentors junior developers in specific areas of expertise. Engages with cross-functional teams to develop applications that meet customer needs. Uses independent judgment and applies programming/software principles, theori...

Experience in Herbal extract & Vet.Products formulations. Must have knowledge o Vertical Extractor, ver. evaporator, filtration, Rotation vacuum paddle dryer, vacuum tray dryer, cooling tower, chiller, multi milling, shifter etc

Your Day-to-Day Tasks Include: 1. Initiating first level contact with Inbound and Outreach leads. 2. Creating and executing an outreach strategy in collaboration with the PDR Managers and PDR team leads.

R&D (Synthesis) -Agrochemical Industry-Saykha,Gujarat. Capital Placement Services Industry IT Software - Application Programming / Maintenance Qualification M.Sc Key Skills Green Field Projects UPLC Gujarat R&D (Synthesis) PDR R&D Develo

You will be responsible for the formulation development of Pharmaceutical and Nutraceutical products including tablets, capsules, effervescent tablets, sachets powders, and liquid formulations. This involves conducting literature search and patent search for the formulation, as well as developing cost-effective and fast production processes along with stable formulations. You will be required to create MFR and relevant specifications, facilitate tech transfer, and maintain documentation. Additionally, you will need to address any ongoing issues in the existing formulations. The ideal candidate should have 7 to 10 years of experience in this field. If you are interested in this opportunity, p...

Role & responsibilities Job description Perform protocol for drug excipient compatibility studies and submit the protocol for review and approval Complete lab. experiment hands-on independently (Lab scale to exhibit batch and query handling). Dosage forms experience: Injectables predominantly more than 90% in career. Perform formulation development activities on differentiated formulations and innovative technologies as part of product development. Carry out /Support Scientific literature search (CVM/USFDA/Daily-med/publications). Follow good laboratory practices, good documentation practices (online LNB writing) and maintain the logbooks and forms for equipment/instruments. Compilation, int...

Roles and Responsibilites 1.In process Quality Assurance activity in Production and warehouse area 2.Provide line clearance as per SOP 3.Monitoring and QA rounds in production and Warehouse 4.Sample verification against TRF / BPCR 5.Carry out Semi-finished / finished product sampling for release, stability study and control samples 6.To send samples along with TRF to Quality control laboratory 7.Participate in media fill, process validation, cleaning validation activities as per requirement 8.Timely communication and co-ordination with all the stake holders 9.Participation in Change control, Deviation & Investigations as per requirement 10.Preparation / review of documents like; SOPs, risk a...

Develop SOPs for production, filling, packaging & QA/QC; ensure FDA, EU, BIS & Drug Act compliance; conduct audits; review BMR, BPR & MFR; implement QMS; train staff on GMP/GLP; manage labelling, claims & documentation for regulatory compliance.