Executive - Production

**The**Opportunity**:
**The Opportunity**:
Ensure uninterrupted product manufacturing by executing production activities aligned with established quality and operational standards. Drive consistency and efficiency through adherence to defined procedures and responsibilities.

**What we are looking for**:

- ** Experience**: Min 05-06 years of Exp of relevant experience
- ** Educational Qualification**: Postgraduate or above in Sciences - Life Science /Biotechnology Microbiology/Chemistry /Pharmacy.
- Manage the workforce for manufacturing of IVD products manufacture at Dehradun plant through a staff of both professionals and contract labor.
- Supervision of assigned work/operations of Rapid/ELISA/Biochemistry/Hematology manufacturing process and maintains their logbook.
- Ensures that production plans are completed by a scheduled time to achieve fill rate target.
- Prepare relevant documents (BMR/BPR/SOP).
- Compiles and analyses production documents and records.
- Responsible for material/bulk reconciliation after batch completion.
- Implements cost-saving strategies and techniques to meet Operational Excellence
- Conduct training.
- Responsible for preparation and review the deviation investigation report, CAPA and root cause
- analysis.
- Enforce strict safety guidelines and company standards.
- Knowledge and Understanding of MDR 2017 and ISO 13485.
- Drive alignment of Production goals with Avantor overall goals and objectives.

**Technical Skills**
- Sound knowledge of ELISA, Clinical chemistry, Rapid techniques and Hematology
- Skilled in resource allocation to meet tactical demands and strategic business needs.
- Customer (internal and external) driven approach.
- Knowledge of investigations tools.

**Other Skills**
- Time management
- Team player
- Computer skills
- Problem-solving skills
- Effective written, verbal and listening communication skills.
- Must be honest and trustworthy.
- Must be respectful and flexible.

**How you will thrive & create an impact**:

- Manufacturing of CLIA (Chemiluminescence Immunoassay) or FIA (Fluorescence Immunoassay) reagents (Fabrication) as per defined process
- Manufacturing Hematology and Biochemistry reagents as per defined process (Preferable)
- Execute the manufacturing activities on the Production Floor as per schedule.
- Work on manufacturing efficiency for Manual and automation production activities
- Preparing the SOPs for Production processes.
- Guiding/ Supervising/Advising the workers in production.
- Maintaining documents pertaining to daily working schedules.
- Maintaining compliance as per GMP standards
- Collate and analyze data, putting together production reports for manager.
- Providing first Aid to the employees
- Work with manager to implement the company's policies and goals.

**Additional QMS**
- Preparation and review of Department Procedures and Protocols.
- Necessary change controls are initiated & adequately approved before change in any product/

process/design etc.
- Work with managers for the timely completion of investigations & action points for Incidents/CAPA and audit observations.
- Ensure Adherence/Compliance to records management policies and procedures as applicable.
- Conduct the training for workers as and when required.

**Others**
- Ensure safety requirements are in place all the time.
- Maintain basic hygiene of the production floor.
- Ensure Current Good Manufacturing & Good Documentation practices are followed all the time.
- Timely intimation of NC for Investigation and Non-conformance (NC) closure.
- Responsibility may be changed as per the instruction of Production Manager.

**AUTHORITIES (if applicable)**:Authorized initiation of BMR/BPR issuance request. Authorized for ETQ initiation of Procedure, BMR, BPR and SOPs

**Disclaimer**:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position. Avantor is proud to be an equal opportunity employer.

**Why Avantor?**

**Dare to go further in your career.**Join our global team of 14,000+ associates whose passion for discovery and determination to overcome challenges relentlessly advances life-changing science.

**The work we do changes people's lives for the better.** It brings new patient treatments and therapies to market, giving a cancer survivor the chance to walk his daughter down the aisle. It enables medical devices that help a little boy hear his mom's voice for the first time. Outcomes such as these create unlimited opportunities for you to contribute your talents, learn new skills and grow your career at Avantor.

**EEO Statement**:
We are an Equal Employment/Affirmative Action employer and VEVRAA Federal Contractor. We do not discriminate in hiring on the basis of sex, gender identity, sexual orientation, race, color, religiou