21 Manufacturing jobs in Nashik

Company:

Job Purpose
Accountable for the following activities;
GLP compliance, internal audits, Lab Investigations, Lab Safety, EHS, and Risk management related to Quality department and Values & expectation of the Organization.
Support to the production department to meet the manufacturing schedules by timely release of Raw materials / finished products/stability/validation/packaging material/ testing etc.
Key Responsibilities
To ensure testing and release of raw material ,excipient, packing material, microbiological sample, bulk and finished product.
To ensure stability program conducted as per protocol
To support validation team for process validation samples analysis management
To ensure qualification ,calibration and maintenance of all laboratories instruments
To ensure OOS investigation and reporting in time
Control on lab. Related SOPs/PQS/PMSP Reviews as per schedule
Control on Reference standards management require for QC Laboratories
To ensure CAP/ATS compliance
To ensure that the activities in the QC Lab are in compliance with regulatory requirements
To ensure Compliance and inspection readiness
Verify compliance to Good Laboratory practice and Schedule L1of D & C act
To conduct initial assessment of change control raised in area of operation
Ensure monthly L1 audit of EHS/Quality as per schedule to identify gaps & timely closure of actions.
Reduction in the cGMP noncompliance coming from L1/L2/L3/L4 audit and WHO audits
Tracking of staff leave and promote for plan absenteeism. Unplanned absenteeism cases to be handle as per standard procedures.
One on one discussion with staff to maintain discipline and building their capabilities.
Coaching/counseling of staff for adherence to standards related to safety, quality & delivery.
Quarterly Performance discussion with staff and ensure recording of NMS performance in PDP card.
Coordination & monitoring of dept consumables & inventory.
Handling of electronic systems (e.g. Empower, MERP, VQD, VQMS, SLIMS etc.)
Resource management of laboratory to have smooth work function department is done in time.
Ensure procurement for item required for quality department is done in time
Site SQCS contact; ensure adequate QC support in vendor approval process .Timely analysis of purchase samples.
To complete the QMS training in time and ensure the compliance with QMS in your area of operation. To carry out the gap analysis as per the requirement.
To ensure SOPs for area are under control are valid and meets all regulatory and QMS requirements
Risk management for department, Control on risk Log, Preparation of STPs and tracking of risks.
To ensure monthly EHS meeting are happening and issues are discussed and sorted.
Encourage staff for proactively identification of unsafe condition & unsafe behavior. Report it through ZAP process.
Responsible for control on Chemical reagents and special hazards including sensitizers, Sensitizing and Biological agents
Build an culture of reporting safety incidents and its closure within timeline with appropriate CAPA.
To provide and support of EHS activities in Quality control.
To ensure prevention of first aid cases/accident in department.
To promote safety culture in Quality control department.
To participate in RCAs as per requirement
Ensure compliance to GPS principles (LSW, Gemba,3Z etc)
Drive improvement with an approach of Kaizen & CIF.
To ensure continuous improvement in laboratory working and to impart working of QC staff
Support the functional head to establish the activities assigned or identified as and when basis.
To provide authorization/approval of QC documents.
Control on safekeeping of controlled substances in QC laboratory.
Scope of Accountability
Attendance Management.
People Development.
Manpower Planning.
Area Management.
Site critical CIF delivery.
Level 2 audit completion.
Delivery of department budget.
Quarterly OT not exceeding 105 hrs and maintaining OT budget for month.
Ensuring no overdue QMS action in dept.
Educational Background : M.Sc /B.Pharm/ M.Pharm
Job-Related Experience :
14-18 years experience in Pharmaceutical Plant, 10+ years in QC
Acquaintance with respect to job requirements
Advanced knowledge of computer software & potency in use of computer software
Leadership skills
Resource Planning
Problem Solving
Effective communication skills
Ability to build relationships (Team building ) at all levels and across functions.

Hello Visionary!

We empower our people to stay resilient and relevant in a constantly changing world. We’re looking for people who are always searching for creative ways to grow and learn. People who want to make a real impact, now and in the future. Does that sound like you? Then it seems like you’d make an outstanding addition to our vibrant team. Siemens Mobility is an independent run company of Siemens AG. Its core business includes rail vehicles, rail automation and electrification solutions, turnkey systems, intelligent road traffic technology and related services. In Mobility, we help our customers meet the need for hard-working mobility solutions. We’re making the lives of people who travel easier and more enjoyable while constantly developing new, intelligent mobility solutions!

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We value your unique identity and perspective and are fully committed to providing equitable opportunities and building a workplace that reflects the diversity of society. Come bring your authentic self and create a better tomorrow with us.

Make your mark in our exciting world at Siemens.

This role is based in Nashik. You might be required to visit other locations within India and outside. In return, you'll get the chance to work with teams impacting - and the shape of things to come. We're Siemens. A collection of over 379,000 minds building the future, one day at a time in over 200 countries. We're dedicated to equality, and we encourage applications that reflect the diversity of the communities we work in. All employment decisions at Siemens are based on qualifications, merit and business need. Bring your curiosity and creativity and help us shape tomorrow.