2048 Formulation Jobs - Page 21

Role & responsibilities We are looking fresher candidate Preferred candidate profile Male candidate

Job Title Manager -IP prosecution Job Grade G10 Function: Global Business Development Sub-function: IP Litigation Manager’s Job Title: General Manager Skip Level Manager’s Title: Function Head Title: Vice-President Location: Baroda Job Summary Branded and NCE portfolio Management of the branded portfolio from IP perspective Areas Of Responsibility At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. ...

Job Purpose: To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeo...

Title of the Project : Formulation and characterization of diabetic wound healing gauze using PDGF-eugenol nanocomposites for Diabetic foot ulcer (DFU) - A 3D bioprinting approach " Qualification : 1. Post Graduate Degree, including the integrated PG degrees 2. For Engineering / IT / CS - Four Years Graduate Degree. Mandatory Skills : Candidates having hands-on experience in the area of 3D bioprinting/Microbiological work/animal experimentation will be preferred. Strong publication records relevant to the field. Fluent in English, both written and spoken. No. of Vacancies : 1 Sponsoring Agency : ICMR Duration : 1.5 Years

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their busines...

Role & responsibilities: a. Plan, manage, and oversee the work activities of QC and Microbiology laboratories to ensure lab testing provides the highest quality analytical support for manufacturing in a timely and compliant manner, adhering to protocols, cGLP, and safety regulations. b. Manage analytical method validation of products, method transfer, stability studies, and related activities to ensure compliance with regulatory and quality standards c. Provide leadership, management, performance evaluation, and training to all laboratory employees to maintain a competent and motivated team. d. Execute and approve all laboratory operations, including reviewing and investigating any laborator...

The incumbent will be responsible for carrying out manufacturing activities in the Oral Solid Dosage (OSD) production area, including Compression, Coating, Encapsulation, and Bottle Packing (Primary & Secondary). The role ensures adherence to GMP, safety, and quality standards during all production processes. Sound knowledge of GMP documentation and BMR/BPR . Hands-on experience in compression, coating, capsule filling, and bottle packing operations . Basic understanding of equipment calibration, validation, and maintenance practices . Strong focus on quality, safety, and compliance . Good communication and teamwork skills. Role & responsibilities Preferred candidate profile

Key Responsibilities To design and develop new & disruptive innovative products & applications , within and outside existing standards, by initiating, guiding, and monitoring projects & validation in active coordination with marketing and to guide and monitor implementation in coordination with plants Product cost optimization through value added projects : Identify, develop & drive a product centric value creation projects to optimize product cost through optimization of slag & Fly Ash | utilization of alternative raw material | utilization of various industrial wastes like LD slag, Pb& Zn slag, Cu- slag, red mud & paper sludge | optimization of SO 3 content | Gypsum Mix | Grinding Aid form...

supporting and maintaining production machinery, assisting in the design and installation of new equipment and ensuring compliance with Good Manufacturing Practices (GMP) . Key responsibilities include troubleshooting machinery, assisting with performing preventative maintenance, and helping with project coordination related to mechanical systems like HVAC and cleanrooms. Preferred candidate profile: Candidate must have B.E in mechanical, should have sound knowledge about pharma machinery . Passout Bach on or before 2025 only.

Key Job Responsibilities Lead and manage product development activities within the FRD department, ensuring timely execution of new and patentable formulations. Oversee product development projects aligned with company strategy and market requirements. Plan, monitor, and control project timelines, resource allocation, and documentation to achieve defined goals. Ensure all development activities comply with organizational standards, regulatory requirements, and quality guidelines. Guide and mentor the team in formulation design, process development, and technical troubleshooting. Review scientific literature, evaluate research data, and support decision-making for new product development. Coo...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: QC Quality Control Experience: (02 07 Years) •HPLC/ IP/ FP/ RM/ Validation/ Stability/ GC/ Micro-biology ARD - OSD Experience: (02 06 Years) •HPLC/ FG/Analytical Method validation/ Stability PACKING Experience: (01-06Years) •Blister Packing, Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) PRODUCTION Experience: (01-06Years) •Compression, Granulation, Coating, QUALIFICATION : ITI, Diploma, B.Sc, B.Com, M.Sc, B.Tech, B. Pharm, M.Pharm with relevant experience DESIGNATIONS: Operator, Jr. Officer, Officer & Jr.Executive NOTE: Offering a Joining bonus only for QC Depart. for Immediate Joiners Instrument experience in HPLC / GC ...

Manage day-to-day production operations ensuring smooth functioning of the production floor. Monitor and optimize production processes to meet monthly capacity and quality targets. Identify areas for process improvement and implement efficiency-enhancing measures. Work closely with the R&D department to analyze product stability issues, troubleshoot failures, and support formulation improvements. Understand machine automation requirements and support upgrades to enhance productivity. Ensure product quality standards are consistently met through strong process controls. Prepare and maintain documentation required for ISO audits and BIS compliance. Ensure adherence to safety, hygiene, and regu...

Job Summary The Global Partner Manager will be dedicated to leading a Global GSI Partner, dedicated to building pipeline and partnerships with NetApp’s Global System Integrator based in India. This role will work across all lines of business at NetApp and our largest strategic partners to help define and lead the acceleration of joint sales, joint business planning, and the development of unique solutions to help solve our customers' biggest challenges. As the India leader, your deep and broad GSI partner sales experience, executive presence, and in-depth understanding of the processes, systems, and tools will ensure a “partner-focused” go-to-market strategy. In this role, you will lead a cr...

Note: Walk In Interview at Vapi Date: - 23-11-2025 (Sunday) Designation: Technical Associate Location: Sarigam, Valsad-Gujrat Experience: 2 to 8 years in Fomulation Qualification: ITI/Diploma Required Candidate profile Experience in HVAC / Plant Maintenance in Formulation Plant

Applications are invited for the post of Project Research Scientist-I (Non-medical) for an ICMR, Government of India funded project in the Centre for Nanobiotechnology Vellore Institute of Technology (VIT), Vellore, T.N, India. File No: EM/Dev/SG/144/2109/2023 Title of the Project : “Formulation and characterization of diabetic wound healing gauze using PDGF-eugenol nanocomposites for Diabetic foot ulcer (DFU) – A 3D bioprinting approach " Qualification : 1. Post Graduate Degree, including the integrated PG degrees 2. For Engineering / IT / CS - Four Years Graduate Degree. Mandatory Skills : Candidates having hands-on experience in the area of 3D bioprinting/Microbiological work/animal exper...

Job Description: Sales & Marketing-Formulation (South Africa , Zimbabwe , Botswana) Role Objective :- Lead the Marketing and Sales function. Develops marketing and sales strategy to increase market share and profitability. Organizes and controls implementation of marketing and sales tactics. Handles major sales and negotiation; appoints both agents and distributors and works with them. May also be responsible for developing new business, either by introducing new products or by entering new markets. Key Responsibilities: Budget achievement P & L. Primary Sales Order generation Ex-India sales for Assigned Geographies mainly South Africa, Zimbabwe, Botswana Countries 1. Primary Sales & Demand ...

Company: Aurobindo Pharma APL HC-4 (Naidupeta Location) Work Location: Naidupeta (Plant) | Walk-in Venue: Hotel palm grove, East Sikkim Interview Date & Time: Saturday & Sunday, 22 November 2025 & 23 November 2025| 09:00 AM 05:00 PM Open Positions Production OSD (Granulation/Compression/Coating/Capsule Filling) • Executive/Sr. Executive: B.Pharm/M.Pharm, 2-6 years • TA/Sr. TA: ITI/Diploma/Degree, 2-8 years Production Oral Liquid / Nasal Spray • Executive/Sr. Executive: B.Pharm/M.Pharm, 2-6 years • TA/Sr. TA: ITI/Diploma/Degree, 2-8 years Packing OSD (Blister/Bottle) • TA/Sr. TA: ITI/Diploma, 2–8 years QC – IP/FP, Stability, Nasal • Executive/Sr. Executive: B.Pharm/M.Pharm/M.Sc, 2–6 years QA ...

Job Description: > Ensure 100% compliance with all regulatory laws for all SDL products. > Manage and control the annual regulatory compliance budget. > Maintain and archive regulatory documents and communication history. > Analyze changes in regulatory frameworks and guide internal teams on required process updates. > Develop strategies for regulatory compliance in international markets. > Liaise with Regulatory Authorities and Government Bodies. > Collaborate with cross-functional teams during product development, testing, and commercialization. > Conduct internal training sessions on the latest regulatory requirements. Who Can Apply? > B.Pham,BAMS/MD with PG in Regulatory Affairs OR PG in...

Head Engineering (Pharma OSD) Manage maintenance, utilities, HVAC, water systems, CAPEX, TPM, compliance (USFDA/MHRA/WHO), energy efficiency & safety. Lead team, ensure uptime, audit readiness & cost control in formulation plant. CV @ 9106329670 Food allowance Office cab/shuttle Annual bonus Provident fund Health insurance

Job Title: Senior Manager – Production (Complex Injectables) Business Unit: Sun Global Operations Job Grade G9B Location : Baska (Baroda) At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: Monito...

We are seeking a dynamic and experienced Assistant Manager / Manager (F&D) to lead product development, formulation, and innovation activities within our Food Supplement division.

JD for Shift in Charge: Shift Handling Manpower Handling Proper SOP following in down line Safe operation handling R.M issue in SAP System Training gives to downline Timely target achieves of production Regular duty attends Routine maintenance work Running Problem Solving Document work JD for Production-Supervisor Candidate with DCS Experience is required Responsible to keep document online. Responsible to perform all activities should be as per SOP. Responsible for distribution of work to workers. Responsible for use of utility and purified water as per requirement. Responsible for to ensure scrubber system & vacuum system before start operation. Responsible for to ensure Raw materials with...

Formulation (Tablet): Technician (ITI/ SSC/ HSC): Fette & Sejong Compression, Glatt & PAM Glatt Coater, Viswill Camera Inspection Machine & Granulation equipment operator Technical Assistant (B. Pharm): Experience in Online documentation, BMR, QMS. Formulation (Packing): Technician (ITI/ SSC/ HSC): BQS / Romaco Blister Packing Machine, Auto Cartonator Machine, CV and Contact Bulk packing machine operator Technical Assistant(B. Pharm/ B.Sc): QMS, Track & Track system (Optel / ACG) with serialization system

ear Candidate, We are seeking a Senior Executive/ Assistant - Regulatory affairs Europe) to join our team, He/ she will be responsible for Dossier compilation, preparation, Life cycle management, Pre approval, Post approvals. based at Govandi Location. Markets : Europe Dosage Form : OSD/ Sterile Key Responsibilities: Collate/prepare and file dossiers in a timely and accurate manner for formulations/ drug products to get licenses from various targeted markets. Prepare the checklist for documentation for regulatory filings as per current regulatory requirements (country specific). Collate and conduct first-level review/overview of relevant standard technical documentation like stability, TTD, ...

Job Title: Senior Executive/Manager 2 Job Grade G11B/G11A Function: Global Business development Sub-function: IP Prosecution Manager’s Job Label: Senior Manager - 1 Location: Baroda Job summary/Areas Of Responsibility At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ...