11 Capsule Jobs

As the Head of Quality Control at a leading Pharma MNC located in the Chandigarh Vicinity, you will be responsible for overseeing the quality control operations of highly regulated plants, specifically focusing on tablet/capsule/pallets/OSD products with a preference for injections. With over 20 years of experience in the industry, you will demonstrate a track record of excellence in maintaining MHRA and EUGMP profiles, along with multiple successful audit exposures. In the realm of Quality Assurance, you will showcase a deep understanding of the latest updates outlined in the ICH Q9 guidelines. For Quality Control, you will exhibit proficiency in the Updates related to ICH Q2R2 Analytical method validation. Moreover, your leadership skills will be put to the test as you manage a large team, drawing upon your prior experience in handling sizable teams effectively. A key requirement for this role is a proven track record of stability, demonstrating your ability to navigate challenges in the pharmaceutical quality control landscape with resilience and expertise.,

The position of Head of Quality Assurance at a Leading Pharma MNC in Chandigarh Vicinity offers a competitive salary of up to 60 LPA. As a qualified candidate, you must possess over 20 years of experience in managing highly regulated plants, with a strong focus on Tablet/capsule/pallets/OSD products, and preferably injections as well. Your expertise should include an excellent MHRA and EUGMP Profile, along with a track record of multiple successful audit exposures. In the realm of Quality Assurance (QA), you are expected to be well-versed with the latest updates in ICH Q9 guidelines. Additionally, in Quality Control (QC), familiarity with Updates in ICH Q2R2 Analytical method validation is crucial. Your experience should also demonstrate proficiency in handling large team sizes and showcasing proven stability in your previous roles. If you meet these mandatory requirements and are ready to take on a leadership role in ensuring the quality standards of pharmaceutical products, we encourage you to apply for this challenging yet rewarding position.,

Job Location Wada, Palghar Age Below 50yrs Role & responsibilities : Operate the organization as per plan & profitable through strategy planning and execution of a Tablet Capsules Ointment & Liquid section. To meet the manufacturing target within the norms and budget. To motivate all functional department to achieve management goal. To ensure all functional heads are executing their responsibilities are effectively. Review weekly, monthly, quarterly and year planning and budgeting. Operate the plant as per regulatory and Government norms. Handling of production documents and review. Preliminary and first hand knowledge and handling all types of equipment which are used in Tablet/ Capsules/ Ointment/ Liquid manufacturing. Process trouble shooting, new product batches monitoring, RM + PM Planning. Maintaining and updating batch production record online Keeping all documents as required by cGMP, WHO GMP, GLP norms. Handle all production activities including co-ordination with QA / QC / RA / FDA / Store & Maintenance Department. Execution & Monitoring of process validation & Cleaning Validation Batches. Ensuring that all products are manufactured and stored as per WHO-GMP norms. Ensuring product quality is maintained. Others as added and or required in the course & duty.

As a Formulation and Development Officer for our client based in Vatva, Gujarat, you will be responsible for various key tasks. Your primary duty will involve the development of formulations for all dosage forms such as tablets, capsules, ointments, creams, gels, oral liquids, injectables, and novel drug delivery systems for different markets including regulated, domestic, and ROW markets. This includes activities like document review, planning, and conducting stability studies of R&D batches. Additionally, you will be required to provide technical support for the scale-up and technology transfer to manufacturing processes. You will play a crucial role in troubleshooting formulation-related issues that may arise during production, ensuring a smooth manufacturing process. To qualify for this position, you should hold a Bachelors or Masters degree in Pharmacy. If you believe you possess the necessary qualifications and skills for this role, we encourage you to share your updated CV with us. We look forward to reviewing your application and will reach out to you promptly.,

Role & responsibilities 1. Formulation & Development for Emerging Market & Regulated Market 2. Execution of Lab Trial batches & Tech Transfer activities at site. 3. Lab note book writing & documentation ensuring compliance with regulated guidelines. Preferred candidate profile Experience in Tablet, Capsules, Pellets, ER, SR and DR product development for emerging market M.Pharm Only

Oversee end-to-end manufacturing operations to ensure timely production of pharmaceutical products (tablets, capsules, Liquid.) Ensure compliance with GMP WHO and other regulatory guidelines. Enforce OSHA, EHS Team Leadership & Workforce Management Required Candidate profile B.Pharma / M.Pharma with 16+ years experience in Pharma OSD formulation with with 5+ years in leadership roles.

Job Title: Team Leader - Packing (Solid Oral Dosage Forms) Location: Bangalore Department: Packing Reports To: Packing Head Job Summary: We are seeking a highly skilled and results-driven Packing Team Leader to oversee all packing activities related to Solid Oral Dosage Forms, including Blister Packing, Bottle Packing, Sachet Filling Line. The ideal candidate will be responsible for ensuring efficient packing operations that meet quality, quantity, cost, and compliance targets, while adhering strictly to safety and regulatory standards. Key Responsibilities: Lead and manage daily packing operations in Blister Packing, Bottle Packing to meet packing targets effectively and efficiently. Ensure smooth and reliable manufacturing processes through effective planning, resource estimation, and scheduling. Manage and oversee Quality Management System (QMS) activities, including Change Control, Deviations, Investigations, Risk Assessments, CAPA and Market Complaints. Collaborate closely with cross-functional teams such as Production, Quality, and Engineering to ensure seamless packing operations. Ensure strict adherence to Good Manufacturing Practices (GMP), safety protocols, and compliance standards. Qualifications: Bachelor’s/master’s degree in pharmacy. 10+ years of experience in pharmaceutical manufacturing, particularly in solid oral dosage forms. Strong knowledge of GMP, regulatory guidelines, and QMS. Proven leadership and team management capabilities. Excellent communication and problem-solving skill

Dear Respected All, Greeting from Biophore India pharmaceutical Pvt Ltd. (oral solution exp) We have opening for Formulation R&D Department. Position : Executive or Sr Executive 1)Candidate must have knowledge Prototype & Product Development. 2) Must have Literature Search. 3) Scale-up Batches, Exhibit Batches, DOE Experiments. 4) PDR Preparation & Development related documentation. 5) Experience in US ,EU Markets. 6) Preparation of documents form development stage to Technology Transfer Stage. Preparation and Review of SOP,S related to formulation R&D. Good Communication Skills Ref to Friends or colleagues Please share update resume: careers@biophore.com Total Exp : Current CTC: Exp CTC: Notice Period: Current Designation

Packing Officer/Packing Executive: 0-5 yrs Salary package: 2.0 to 4.0 LPA Location: Dahej Company: Pharma API WP: 7383005000 Required Candidate profile Knowledge as packing officer at pharma, api, chemical or food companies prefer. Fresher with knowledge of packing can also apply.

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage