Brooks Steriscience hiring for multiple roles in Production

At Brooks Steriscience Limited, we are committed to excellence in pharmaceutical manufacturing and quality assurance. Located in the vibrant region of Vadodara, Gujarat, our state-of-the-art facility specializes in API and Sterile API production, adhering to the highest standards of GMP and FDA regulations.

Brooks Steriscience Limited
Block No 61/62, Village Manglej, Nareshwar Road, Tal Karjan, Dist: Vadodara, Gujarat

Position: Executive (Documentation) – Production Department

Qualification:

• MSc/BSc (Familiarity with GMP, FDA regulations, and other relevant quality standards)

Experience Required:

• 5 to 8 years in Pharma Industry (API Plant)

Key Responsibilities:

• Manage Drug product manufacturing and QMS compliance
• Prepare and revise Master Production/Formula Records (MFR/MPR), Batch Manufacturing/Production Records (BMR/BPR), SOPs, Trend, Qualification documents, Protocols, and Reports
• Manage the change control process for production documentation, ensuring changes are properly documented, approved, and communicated
• Effectively implement CAPA
• Proficiency in SAP system
• Prepare for and participate in internal and external audits and inspections related to production documentation and implement audit CAPAs
• Experience in USFDA approved site

Application: Interested candidates should share their most updated CV with the HR Department at archit.upadhyay@brookssteriscience.com

Position: Executive (Sterile API) – Production Department

Qualification:

• B.E. / B.Tech. / B. Pharma / MSc.

Experience Required:

• 5 to 8 years in Pharma Industry (Sterile API)

Key Responsibilities:

• Lead and supervise production teams during assigned shifts, ensuring the effective operation of Sterile API manufacturing processes
• Ensure compliance with Sterile processing procedures, including aseptic techniques, cleanroom protocols, and environmental monitoring
• Implement and maintain practices that uphold the sterility of the production environment
• Enforce adherence to GMP and other relevant quality standards specific to Sterile API manufacturing
• Work closely with the Production Planning team to ensure accurate scheduling and sequencing of Sterile API production activities
• Proficiency in handling critical equipment (Reactors, Filters, ANFD, Powder Filling, Autoclave) and working in a batch process, cGMP environment
• Experience in USFDA approved site and SAP system

Application: Interested candidates should share their most updated CV with the HR Department at archit.upadhyay@brookssteriscience.com

Position: Officer – Production Department

Qualification:

• MSc/BSc

Experience Required:

• 2 to 5 years in Pharma Industry (API Plant)

Key Responsibilities:

• Execute API manufacturing processes under the guidance of senior production staff
• Follow GMP and SOPs to maintain high-quality production
• Accurately document production activities, including batch records, logbooks, and other required paperwork
• Adhere to safety protocols and guidelines to ensure a secure working environment
• Report safety concerns or incidents promptly to the supervisor
• Identify and report deviations, abnormalities, or issues during production processes
• Monitor environmental conditions within the production area to meet specified requirements
• Proficiency in handling critical equipment (Reactors, Centrifuges, Dryers, FBD, Filters, ANFD, Hydrogenator) and working in a batch process, cGMP environment

Application: Interested candidates should share their most updated CV with the HR Department at archit.upadhyay@brookssteriscience.com

Position: Officer/Operator (Sterile API) – Production Department

Qualification:

• MSc/BSc

Experience Required:

• 5 to 8 years in Pharma Industry (Sterile API)

Key Responsibilities:

• Execute Sterile API manufacturing processes according to SOPs and aseptic processing guidelines
• Operate and monitor equipment and machinery involved in Sterile processing
• Adhere to Sterile processing protocols, including gowning procedures, cleanroom behavior, and environmental monitoring
• Maintain awareness of aseptic techniques and contribute to the maintenance of sterility
• Follow GMP and quality standards specific to Sterile API manufacturing
• Proficiency in handling critical equipment (Reactors, Filters, ANFD, Powder Filling, Autoclave) and working in a batch process, cGMP environment
• Contribute to environmental monitoring activities to meet Sterile processing specifications
• Work in shifts and report to the Shift Incharge

Application: Interested candidates should share their most updated CV with the HR Department at archit.upadhyay@brookssteriscience.com

Position: Executive (Shift In Charge) – Production Department

Qualification:

• B.E. / B.Tech. / MSc/BSc

Experience Required:

• 5 to 8 years in Pharma Industry (API Plant)

Key Responsibilities:

• Supervise and lead production teams during assigned shifts, ensuring smooth and efficient operation of API manufacturing processes
• Collaborate with other shift incharges and production managers to facilitate seamless transition between shifts
• Proficiency in SAP system
• Proficiency in handling critical equipment (Reactors, Centrifuges, Dryers, FBD, Filters, ANFD, Hydrogenator) and working in a batch process, cGMP environment
• Provide training and mentorship to production staff on API manufacturing processes, safety protocols, and regulatory compliance
• In-depth knowledge of GMP, safety regulations, and quality standards in API production
• Knowledge and compliance of clean room equipment and area
• Experience in USFDA approved site

Application: Interested candidates should share their most updated CV with the HR Department at archit.upadhyay@brookssteriscience.com

For all positions, please ensure your CV includes relevant experience and clearly outlines your qualifications and responsibilities in previous roles. We look forward to welcoming dedicated and skilled professionals to our team.