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20.0 - 30.0 years
100 - 150 Lacs
andhra pradesh
Work from Office
Oversee the end-to-end manufacturing operations of the three API units Develop and implement long-term operational strategies Ensure compliance with regulatory Manage the cluster's operational budget Ensure site safety, health, and environmental Required Candidate profile Min 20+ years in pharmaceutical/API manufacturing Exp managing multi-unit operations and large teams Knowledge of cGMP and QMS Strong leadership & communication skills
Posted 2 months ago
5.0 - 6.0 years
4 - 5 Lacs
ankleshwar
Work from Office
Follow Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Review scientific literature and patents to identify new product development opportunities. Required Candidate profile Specialty Chemicals / Excipients / Pharmaceutical Field Whatsapp CV on 9724346949
Posted 2 months ago
1.0 - 5.0 years
1 - 3 Lacs
navi mumbai
Work from Office
Desired Candidate Profile Bachelor's degree in Science (B.Sc.) or Master's degree (MS/M.Sc) in a relevant field (e.g., chemistry). 1-5 years of experience in API manufacturing industry with expertise in bulk drugs production. Strong understanding of active pharmaceutical ingredients (APIs) and their applications. Proficiency in handling chemicals safely and following good laboratory practices (GLP). Responsibility for shift activities, online documentation, maintain accurate records of Production activities. Responsibility for process all steps followed as per BMR & SOP and final products meets Quality and Quantity. Responsibility for comply GMP, Safety and regulatory requirements and keep t...
Posted 2 months ago
3.0 - 5.0 years
4 - 6 Lacs
daund
Work from Office
Technical Skills : Operation and troubleshooting of preparative HPLC systems. Column packing, running, and optimizing columns for compound isolation. Sample preparation and purification techniques. Skilled in solvent evaporation, concentration of samples, and handling of temperature-sensitive compounds. Documentation and compliance with GMP standards Preferred candidate profile: Experience : Minimum 3 to 5 years in handling Preparative HPLC systems in API manufacturing or R&D environments Educational Qualification : BE / B-Tech / B.Sc / M.Sc in Chemistry or equivalent
Posted 2 months ago
0.0 - 1.0 years
1 - 4 Lacs
bengaluru
Work from Office
Roles and Responsibilities Assist in API production activities, including cleaning equipment, operating reactors, dryers, centrifuges, filters, and other manufacturing machinery. Ensure adherence to safety protocols and maintain a clean working environment. Perform routine maintenance tasks on equipment and facilities to prevent downtime. Collaborate with team members to troubleshoot issues and optimize production workflows. Requirement- Qualification: B.Sc. Chemistry / Diploma in Chemical Engineering / B.Tech in Chemical Engineering Experience: 02 Years (Freshers ,Apprentices and Interns are welcome to apply) Interested candidate share your resume at preeti.thakur2@cipla.com
Posted 2 months ago
5.0 - 10.0 years
12 - 16 Lacs
hyderabad
Work from Office
Serve as a liaison between CMs and Lilly. Provide quality oversight of CMs including being the initial point of contact for all quality related issues. Escalate quality issues at CMs to Lilly QA management. Assist in the establishment and revisions of Quality Agreements with affiliates and customers. Provide quality oversight of Lilly/APIEM Quality Plans Coordinate and perform QA responsibilities of API shipments. Participate in regulatory inspection preparations with CMs. Provide on-site support during manufacturing events and inspections. Participate on the Technical Review Board Evaluate and disposition API batches, if required. Ensure that documented checks have been completed for the Ce...
Posted 2 months ago
0.0 - 1.0 years
2 - 3 Lacs
bengaluru
Work from Office
Role & responsibilities Hiring BSc - Chemistry , Diploma in Chemical Engineering freshers for the Production department (API industry ) . Only male candidates can attend Walkin interview .
Posted 2 months ago
5.0 - 9.0 years
0 Lacs
udaipur, rajasthan
On-site
Role Overview You will be joining Bal Pharma Limited, a Bangalore based company known for specializing in API, Intermediates, and Finished Formulations. With 6 state-of-the-art manufacturing facilities approved by various international regulatory bodies, the company supplies products to over 60 countries, establishing a strong presence in the industry. Key Responsibilities - Oversee quality control processes for API manufacturing - Ensure compliance with regulatory standards - Conduct inspections and audits to maintain quality standards - Manage and lead a team of QC professionals effectively Qualifications Required - Experience in quality control processes and regulations - Knowledge of API...
Posted 2 months ago
3.0 - 8.0 years
2 - 7 Lacs
aurangabad
Work from Office
Responsibilities: Conduct HPLC, GC, UV, water analyses per BMRR. Implement change controls, manage deviations. Perform API manufacturing, intermediate handling, SRP processing.
Posted 2 months ago
0.0 - 5.0 years
2 - 3 Lacs
bharuch, valsad, vapi
Work from Office
Qualification: B.Sc / M.Sc / B.Pharma Experience: 2 – 4 Years in Pharma Production Location: G.I.D.C., Kabilpore, Navsari Shift Timings: 8 Hours Duty Salary: Up to 3,00,000 CTC Gender: Male Industry: Pharmaceuticals – Manufacturing 9081799800 Required Candidate profile Experience in pharmaceutical manufacturing operations Strong understanding of GMP and regulatory expectations Only candidates from Navsari/South Gujarat region will be considered
Posted 2 months ago
10.0 - 20.0 years
8 - 14 Lacs
navi mumbai
Work from Office
Oversee Quality Control for API manufacturing, ensuring GLP, GMP, and regulatory compliance. Lead QC team, manage validations, audits, stability studies, and documentation from raw material to finished product with focus on quality excellence.
Posted 2 months ago
16.0 - 23.0 years
70 - 90 Lacs
andhra pradesh
Work from Office
Hiring a Unit Operations Head for its greenfield API manufacturing facility API production Ensure compliance with global regulatory standards Lead process improvement & scale-up Manage budget & cost efficiency Lead and develop cross-functional teams Required Candidate profile 18+ years in API/Pharma manufacturing ONLY - Operational Excellence Strong Plant Operations leadership exp, Regulatory Compliance Proven track record with USFDA/MHRA audit Age below 50 years preferred
Posted 2 months ago
16.0 - 20.0 years
15 - 20 Lacs
raichur
Work from Office
Roles and Responsibilities Review documents from various departments to compile regulatory submission. Oversee drug master file for submission to regulatory authorities, including updates, amendments, and revisions as required. Draft both the applicant and restricted parts of DMF s to ensure regulatory complience. Coordinate with CFT to address deficiency and feedback from RA and customers. Conduct CFT meetings to ensure timely responses to regulatory deficencies and customer inquires. Provide regulatory guidance to product development teams and attend technology transfer meetings to support compliance. Respond promptly to technical queries from regulatory bodies and customers.
Posted 2 months ago
0.0 years
1 - 2 Lacs
bengaluru
Work from Office
Preferred candidate profile B.Sc Chemistry 2024/25 passed out candidates are preferred Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy
Posted 2 months ago
3.0 - 6.0 years
10 - 20 Lacs
hyderabad
Work from Office
Job Summary We are seeking a dynamic and experienced Scientist in Process Engineering in Active Pharmaceutical Ingredient (API) development with proven expertise in scaling up or down technologies to meet production demands. Proficient in Process and Chemical Engineering, adept at troubleshooting complex projects, facilitating technology transfer, and optimizing operations. Roles & Responsibilities You will be responsible to review of journals and patents. You will be responsible for feasibility study of the Process, Process Optimization,Lab Validations, Technology Transfer to plant and identify and evaluate the reaction parameters You will be responsible for staying up to date with relevant...
Posted 2 months ago
10.0 - 18.0 years
14 - 18 Lacs
tarapur
Work from Office
We’re looking for an experienced Manager – Fermentation (Production) with 10–15 years of experience in the API Pharma industry. Qualification: M.Sc./B.Sc. in Microbiology
Posted 2 months ago
10.0 - 18.0 years
14 - 18 Lacs
tarapur
Work from Office
We’re looking for an experienced Manager – Fermentation (Production) with 10–15 years of experience in the API Pharma industry. Qualification: M.Sc./B.Sc. in Microbiology
Posted 2 months ago
18.0 - 25.0 years
16 - 20 Lacs
vapi
Work from Office
Job Title: Head Engineering & Maintenance Location: Vapi Number of positions : 1 Reporting To: Sr. VP Operations Department: Engineering & Maintenance Purpose of the Role To provide strategic leadership and operational excellence in managing plant engineering, utilities, and maintenance to support uninterrupted, compliant, and efficient API manufacturing operations. The role combines strategic engineering initiatives (capex, regulatory readiness, energy optimization) with maintenance operations (equipment reliability, preventive maintenance, troubleshooting), ensuring cGMP compliance and readiness for regulated markets. Accountability Tracks 1. Strategic Engineering Develop and execute engin...
Posted 2 months ago
1.0 - 4.0 years
2 - 6 Lacs
bengaluru
Work from Office
Role & responsibilities We are looking for candidates who has hands on work experience in the API manufacturing sector to handle API Production activities like intermediate , Clean room , Second line shift incharge role . Also we are hiring fresh graduates who have passed in 2020 and above . Preferred candidate profile Freshers - BSC /Diploma in Chemical Engineering (Only male ) Junior officer & Officer - BSC ,MSc in Chemistry
Posted 2 months ago
16.0 - 20.0 years
15 - 20 Lacs
raichur
Work from Office
Roles and Responsibilities Review documents from various departments to compile regulatory submission. Oversee drug master file for submission to regulatory authorities, including updates, amendments, and revisions as required. Draft both the applicant and restricted parts of DMF s to ensure regulatory complience. Coordinate with CFT to address deficiency and feedback from RA and customers. Conduct CFT meetings to ensure timely responses to regulatory deficencies and customer inquires. Provide regulatory guidance to product development teams and attend technology transfer meetings to support compliance. Respond promptly to technical queries from regulatory bodies and customers.
Posted 2 months ago
12.0 - 17.0 years
12 - 14 Lacs
ahmednagar
Work from Office
Daily Review of Shift Report & Utility Logbooks Allocation of work to sub-ordinates & contractors as per priorities Ensure efficiently supply of utilities as per production requirement Ensure safety & statutory compliances of departmental activities. Execution of Preventive Maintenance of equipment s as per schedule & updation of records in System. Spares management and ensure availability of critical spares. Attending major breakdowns and preventive maintenance. Execution of planned modification work. Preparation of documents of new equipment s like protocol, history card, P.M. Schedule etc. Effective implementation of Energy Conservation projects. Audit Preparation as per cGMP requirements...
Posted 2 months ago
10.0 - 18.0 years
8 - 16 Lacs
navi mumbai
Work from Office
Role & responsibilities 1. IPR patent evaluation 2. Selection of route of synthesis with costing. 3. Well know about updated guideline of Nitrosamine and GTI. 4. Expert in multi-step organic synthesis 5. Expertise in plant equipment selection, product / process stabilization 6. TTD preparation 7. Expertise in characterization 8. Expertise in Impurity synthesis 9. Documentation required for cross functional team.
Posted 2 months ago
1.0 - 2.0 years
2 - 6 Lacs
india, bengaluru
Work from Office
Preferred candidate profile Diploma in Chemical Engineering / B. Sc Chemistry with minimum 1 year of experience in API Production Recruiter Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy
Posted 2 months ago
2.0 - 6.0 years
2 - 5 Lacs
vasai, satara, virar
Work from Office
Handling Batch process and process equipment, manpower handling, following safety rule. Responsible for consumption of Raw material, yield and quality of intermediate, semi-finished, finished product. Online BMR, BPR and ECR, Daily Records checking.
Posted 2 months ago
20.0 - 24.0 years
0 Lacs
hyderabad, telangana
On-site
Role Overview: As the Head of Engineering & Maintenance at a large-scale API pharmaceutical plant in Digwal, Hyderabad, you will be leading all engineering and maintenance operations. Your primary responsibility will be to ensure the optimal performance, reliability, and compliance of plant equipment, systems, and facilities. Your extensive experience in API manufacturing, expertise in CGMP, FDA regulations, and managing regulatory audits will be crucial in developing and executing maintenance strategies, driving continuous improvement, managing OPEX budgets, and leading a high-performing team to ensure safe, efficient, and compliant plant operations. Key Responsibilities: - Lead, manage, an...
Posted 2 months ago
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