2043 Formulation Jobs

**Job Description:** As the Head of Product Innovation at WHYNutritions, you will lead the research, formulation, and development of the company's food and supplement portfolio. Your primary focus will be on translating credible science into products that enhance everyday nutrition while ensuring taste, shelf life, and practicality. This role provides a high level of ownership and is perfect for individuals aiming to create a significant impact at the nexus of health, food, and science. **Key Responsibilities:** - Lead the formulation and development of functional foods, fortified staples, snacks, and clean-label supplements. - Design product specifications for nutritionally relevant foods w...

Role & responsibilities Ensure that all the required inspection and tests are carried out in accordance with the laid down procedures and techniques. Ensure that quality assurance personnel take necessary samples that they require using the correct sampling procedures. Ensure that test methods are strictly adhered to and test reports are forwarded to the designated authority. Identify and organize calibration of inspection, measuring and test equipment to maintain their continued suitability. Ensure timely corrective action on non-conformities appearing in the system and institute preventive actions to eliminate recurrence of non-conformities. Ensure proper quality of milk is received from t...

Role & responsibilities Lead the strategic planning and execution of all outsourced production activities. This pivotal role ensures that external manufacturing partners meet the company's quality standards, production schedules, and financial objectives. Manage vendor relationships, negotiate contracts, and drive continuous improvement initiatives across the third-party manufacturing network. Preferred candidate profile A minimum of 15 years of experience in the manufacturing sector, with significant experience in contract or supply chain management.

Role & responsibilities Opportunity identification and selling across all product segments and industry verticals Map the total revenue product wise and region wise Analyze the current market demand and potential products to offer New customer acquisition across all product categories Assist team with data, technical inputs and visits wherever required Prepare and discuss the annual business plan with management Marketing Attend Exhibitions, seminars Develop and implement latest Marketing collaterals Brochures, Digital presence Prepare Marketing Budgets Carry out marketing activities based on approved budgets Sales Process management Establish and review Enquiry generation to Order Confirmat...

Responsible for developing and managing quality assurance systems, ensuring product quality, GMP compliance, documentation control, audits, regulatory adherence, deviation handling, CAPA implementation, cross-functional coordination. Required Candidate profile B.Pharm/M.Sc graduate with 4–5 years QA experience in pharma/nutraceutical manufacturing. Certified in GMP/WHO-GMP, skilled in documentation, audits, CAPA, compliance, and quality system management.

Walk In Drive for Production OSD Department In Formulation Division @ Mekaguda Qualification :- Diploma | B Tech | B Sc | B Pharmacy | M Pharmacy Experience:- 0 to 10 Years Interview Date:- 03-01-2026 (Saturday) Interview Time:- 9.00AM TO 2.0PM Work Location :- MSNF- IV, Mekaguda Venue Location :- MSN Laboratories Pvt Ltd,. Formulation Unit-04-Mekaguda 37XJ+W82, Mekaguda, Telangana 509228 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidates those who have experience in Manufacturing:- Production QMS (Equipment Qualification )|Production QMS| Granulation| C...

Formulation Development of Solid, liquid orals, topicals, parenteral etc., dosage form of various markets Scale up, Technology Transfer along with its proper documentation of allocation products of various market. Monitoring Stability data. Required Candidate profile Should have 4+Years of experience in OSD Formulation.

We are looking for a highly skilled and experienced Production Approved Chemist (DPI) to join our team at Career Care. The ideal candidate will have a strong background in chemistry and experience in the field of DPI. Roles and Responsibility Develop and implement new methods for analyzing and testing DPI products. Collaborate with cross-functional teams to ensure smooth production operations. Conduct regular audits to ensure compliance with quality standards. Troubleshoot issues related to product development and manufacturing. Maintain accurate records of test results and product data. Ensure all products meet required specifications before release. Disclaimer: This job description has bee...

We are looking for a highly skilled and experienced Regulatory Affairs Associate III to join our team. The ideal candidate will have a strong background in regulatory affairs and excellent analytical skills. Roles and Responsibility Develop and implement regulatory strategies to ensure compliance with industry standards. Collaborate with cross-functional teams to identify and mitigate regulatory risks. Conduct thorough analysis of regulatory requirements and develop effective solutions. Prepare and review regulatory documents, including submissions and reports. Ensure timely and accurate completion of regulatory tasks and projects. Stay up-to-date with changing regulatory requirements and in...

We are looking for a highly skilled and experienced professional to join our team as an Associate II in Complex Gx Regulatory Affairs. The ideal candidate will have a strong background in regulatory affairs and excellent mentoring skills. Roles and Responsibility Develop and implement complex regulatory strategies to achieve business objectives. Collaborate with cross-functional teams to ensure compliance with regulatory requirements. Provide expert guidance on regulatory matters, including Gx regulations. Conduct thorough analysis of regulatory data to identify trends and areas for improvement. Mentor junior team members to enhance their knowledge and skills. Stay up-to-date with changing r...

We are looking for a highly skilled and experienced professional to fill the role of Deputy Manager - International Marketing SCM. The ideal candidate will have a strong background in supply planning, demand planning, and formulation. Roles and Responsibility Develop and implement effective international marketing strategies to drive business growth. Collaborate with cross-functional teams to identify new business opportunities and expand existing relationships. Analyze market trends and competitor activity to inform marketing decisions. Manage and optimize supply chain operations to ensure timely and cost-effective delivery. Identify and mitigate risks associated with international marketin...

Dear All, We are seeking a highly motivated and talented STP and Specifications Specialist to join our innovative team. The ideal candidate will have a strong foundation in formulation development as well in Analytical Development. Location: Hyderabad(Dulapally) Required Experience: 4-7 Years Key Responsibilities: Preparation of Raw materials, In-process and Finished product specifications and standard test procedures. To review/revise/obsolete the Raw materials, In-process and Finished product specifications and standard test procedures as per requirements in DMS. Handling of pharmacopeial updates. Handling of Quality notifications like CCNs, Incidents, Events etc., Preparation or revision ...

Walk-in @ Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Engineering - (Instrumentation / Process Equipment Maintenance/HVAC) (Senior Executive / Executive / Senior Officer/ officer/ Junior Officer) Experience - 02 to 10 Years Qualification BE / B Tech / Diploma Injectable – Manufacturing & Packing (Executive/Senior Officer / Officer/Junior Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Diploma OSD – Manufacturing & Packing (Seni...

Job Purpose: To execute and support injectable manufacturing operations in compliance with cGMP, SOPs, and regulatory requirements to ensure safe, high-quality sterile products. Key Responsibilities: Execute day-to-day injectable manufacturing operations including: Vial / Ampoule / PFS filling Terminal sterilization / aseptic operations Operate and monitor equipment such as: Autoclaves, Tunnel, Filling Machine, Washing Machine Ensure adherence to cGMP, SOPs, safety, and data integrity Maintain and complete Batch Manufacturing Records (BMR/BPR) Coordinate with QA, QC, Engineering, and Warehouse teams Perform line clearance, equipment cleaning, and changeover activities Participate in media fi...

Roles and Responsibilities Should Have Formulation Experience. US /EU/CA Regulatory Affairs. Submission Drafting/ Compilation/ Publishing of dossiers for US/EU/CA Submissions. Response to information request/ Deficiencies from US/EU/CA in timely manner. Injectable Dosage Forms & Complex Generics Post approval Supplements, Annual Reports. To update cross functional teams for different regulatory compliance & requirements Desired Candidate Profile Perks and Benefits

Roles and Responsibilities 1. Preparation, Compilation and Review of dossiers in CTD/country specific format for ASIA or LATAM or AFRICA or MENA & CIS Regions. 2. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. 3. Manufacturing Site GMP Inspection supports with Customers & Cross Functional Departments. 4. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. 5. Participating in calls with agents/partners for submission of Dossiers and further updates or r...

Role & responsibilities Required for Quality Control(Formualtion) Quality Control(QC)- Need 2 to 5 years of experience. *Method validation/Method transfer. *Analysis of Finshed Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

Roles and Responsibilities Should Have Formulation Experience. Having vacancies in RoW (ASIA , MENA, LATAM, AFRICA) Regions And US/EU Region Responsible for product registration RoW (ASIA , MENA, LATAM, AFRICA) Regions or EU region Preparation, compilation and review of dossiers for region in eCTD/CTD/country specific format. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. Responding to queries with in...

Role & responsibilities • All Types of Consumables for SEZ Unit Chemicals, consumables • Inter Unit Transfers • QC Chemicals, Production Consumables Micro Biology Consumables, EHS & Eng maintenance • Send Enquiry for all vendors for Chemicals /Consumables materials • RFQ Comparisons for Consumables, Raw water, oil, & Gases • Materials delivery follow up as per PPIC-plant requirement • PO Creation for Chemicals / Consumables. PO Approvals Follow up with Approver. Approved PO's send to concern Vendors • New Vendor Code Creation & MPN Code creation • MPN Follow-up with DQA & PDD • Documents follow-up with vendors for VQ & PQ process. • Advance payment Request (DP), Advance & Overdue payments fo...

Roles and Responsibilities Should handle a team of 4-10 members. Must have experience into formulations US - ANDA/NDA and EU Generic/Hybrid applications. Should be familiar with oral solids and parenteral dosage forms. Should familiar with pre and post approval regulatory activities. Should handle the customer and Agency queries. Should handle other regulatory activities based on organization need. Should support plant RA activities and other CFTs as needed. Desired Candidate Profile Perks and Benefits

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....

Roles and Responsibilities Should Have Formulation Experience. 1. Responsible for product registration in ROW (AFRICA, ANZ, ASIA, LATAM, CIS &, MENA). 2. Responsible and involving in the regulatory audits and coordinating with the auditors/customers. 3. Preparation, compilation and review of dossiers for RoW region in CTD /country specific format. 4. Co-ordinating with cross functional departments like API, R&D, QC, QA, PDD, Micro for documents required for dossier compilation for initial submission, query responses or other submission like tender activities. 5. Communicating with agents/partners for submission of Dossiers and further updates or requirements if any on product registration. 6...

Role & responsibilities Responsible for handling of CMO projects of solid orals and injectable products from project initiation to commercial launches Responsible for handling of site transfer projects that and will be SPOC for all projects that will be executed at CMO Responsible for preparation of project tracker and monitoring of project timelines as per set milestones Responsible for handling of activities related to new product launches from CMO sites for US/EU & Canada territories Should be able to coordinate with QP labs for method transfer activities and commercial releases Should be able to coordinate between customers, internal cross functional teams and CMO partners for project ac...

Role & responsibilities Required for Quality Control(Formulations) Quality Control(QC)- Need 1 to 5 years of experience. *Analysis of Finished Product & Stability *GLP and LIMS, Documentation Preferred candidate profile Perks and benefits

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....