2 Opening(s)
3.0 Year(s) To 6.0 Year(s)
4.00 LPA TO 5.50 LPA
Position: QA Officer
Location: Saykha near by Bharuch
Experience: 3 - 6 Years
Industries: Chemical
Responsibilities:
Ensure current versions of all GMP documents are in use across departments.
Prepare, revise, and control SOPs and related quality documents.
Implement and enforce Good Documentation Practices (GDP).
Prevent retention of ...
1 Opening(s)
5.0 Year(s) To 7.0 Year(s)
3.00 LPA TO 4.80 LPA
Position: QC Executive
Location: Daman
Experience: 5 - 7 Years
Industries: Pharma
Responsibilities:
Incoming Material Inspection
Inspect and test incoming raw materials, packaging materials, and components as per approved specifications and sampling plans.
Communicate non-conformances to the supplier and QA & Purchase department.
In-Process Quality Control
Perform in-process checks during production (e.g., dimensional ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.00 LPA TO 4.00 LPA
Position: Production Chemist
Location: Mehsana
Experience: 2 - 3 Years
Industries: Pharma - API
Responsibilities:
Report to the Production Manager on daily production activities and progress.
Ensure adherence to Standard Operating Procedures (SOPs) for cleaning and equipment operations.
Comply with Batch Manufacturing Record (BMR) specifications and promptly report ...
10 Opening(s)
1.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.50 LPA
Following GMP during operation of the equipment and handling of products.
Responsible for Operation of moisture analyzer and ERH apparatus.
Responsible for the following SOPS and BMR’S in the area without any deviations.
Responsible for integrity of punches & dies and sieves, screens, finger bags.
Responsible for the Maintenance of change parts and punch ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
3.60 LPA TO 4.20 LPA
The Process Supervisor is responsible for overseeing and managing production processes to ensure smooth operations, adherence to quality standards, and timely output. The role involves supervising operators, monitoring process parameters, troubleshooting issues, and enforcing safety and compliance protocols.
Key Responsibilities:
🔹 Process Management
Monitor daily production processes to ensure efficiency and quality.
Maintain control ...
1 Opening(s)
3.0 Year(s) To 9.0 Year(s)
Not Disclosed by Recruiter
Summary
The Estimation & Proposal Engineer in a pharmaceutical consultancy will be responsible for developing accurate, competitive, and technically-sound cost estimates, proposals, and tender submissions for pharmaceutical projects (e.g. process design, utilities, cleanrooms, HVAC, validation, regulatory compliance, etc.). They collaborate with cross-functional teams (engineering, procurement, quality, regulatory, project management, sales) to ...
1 Opening(s)
6.0 Year(s) To 10.0 Year(s)
4.00 LPA TO 7.50 LPA
Key Responsibilities:•Handling of QMS tools like change control, CAPA, Deviation etc.•Handle QA efficiently and able to maintain documentation as per GMP.•Preparation and maintenance of training schedule and co-ordinate with working staff to establish Procedures, Standards and System.•Preparation of Raw Material and Finished Product specification in accordance with Regulatory Guideline.•Vendor Evaluation, ...
1 Opening(s)
0 To 1.0 Year(s)
1.44 LPA TO 1.80 LPA
Position: Maintenance Trainee (S)
Location: Somnath - Daman
Experience: Fresher
Industries: Pharma
Responsibilities:
Assist in routine preventive and breakdown maintenance of production equipment such as:
Tablet compression machines, blenders, granulators, coating machines, autoclaves, HVAC, AHU systems, etc.
Support utility equipment maintenance (e.g., chillers, boilers, water systems, air compressors).
Learn to ...
10 Opening(s)
2.0 Year(s) To 5.0 Year(s)
1.80 LPA TO 2.40 LPA
Job Description: Production Operator
We are looking for skilled and reliable Production Operators with hands-on experience in API manufacturing. The ideal candidate will be responsible for executing day-to-day production activities, ensuring efficient batch processing, and maintaining GMP and safety standards.
Key Responsibilities:
Perform routine production operations such as batch charging, centrifugation, material handling, ...
5 Opening(s)
1.0 Year(s) To 6.0 Year(s)
Not Disclosed by Recruiter
Responsibilities
Perform and supervise In-Process Quality Assurance (IPQA) OR QA checks during API manufacturing operations.
Conduct on-line review of Batch Production Records (BPR) and ensure adherence to approved procedures.
Ensure sampling, line clearance, and process compliance as per GMP/cGMP norms.
Identify, record, and support resolution of deviations, non-conformances, and quality incidents during manufacturing.
Support quality investigations and prepare required ...