QC Technician Job Vacancy in West Pharmaceutical Services Andhra Pradesh – Updated today

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Full Details :
Company Name : West Pharmaceutical Services
Location : Andhra Pradesh
Position :

Job Description : Requisition ID: 47561
Date: Feb 15, 2022
Location:
Sri City, Andhra Pradesh, IN
Department: Quality
Description:
Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate – which all help contribute to a Healthier World.

At West, we are by the side of patients. The work we do impacts patients’ lives each and every day – our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges. We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $2.14B in 2020. We serve by the side of our community. Giving back is in our DNA—our team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West Without Borders team member-led giving program.

Job Summary:
Responsible for performing inspection of incoming materials/components, In process/semi-finished goods and finished products as per procedure/SOI.

Essential Duties and Responsibilities:

Perform inspection of incoming materials/components, In process/semi-finished goods and finished products as per procedure/SOI.
Maintenance of stock control samples and records.
Ensure all QC equipment’s and measuring tools used are calibrated. Perform routine calibration of QC Equipment.
Responsible to operate in close co-ordination with production functions for testing and analysis.
Preparing and maintaining necessary QC SOI and upgrading same time to time
Ensure all QC related records are maintained as per GMP, GLP, GDP requirements.
Ensure that all operations in your area of responsibilities are comply with GMP, GLP, GDP, ISO 9001 & ISO 15378 etc.,
Release acceptable in-process and finished goods product for further processing.
Understand and follow applicable ISO standards requirements (ISO 15378 and 9001)
Perform review of inspection records to assure product conforms to specifications and proper documentation practices.
Maintain all applicable documents to form batch records
Perform approval of rework and sorted product
Print documents from Master Control
Manage documents related to the Quality System
Segregate nonconforming product
Handle quarantined product and raw materials
Perform and check manual data entry
Generate rejection and deviation reports
Perform trace back investigation of nonconforming raw material and product.
Any other Duties assigned by supervisor.
Quality: The job holder is aware of his/her special responsibility for quality and conducts his/her activities in accordance with the Company quality policy at all times.
Ensure that all operations in your area of responsibilities are comply with GMP ISO 9001 & ISO 15378 (as per current version)

SOI: The job holder is aware of all relevant SOIs as per Company policy as they are related to the position covered by this Job Description.

Safety: The job holder is aware of his/her special responsibility towards health and safety in accordance with the company’s safety policy at all times;
Proper use of Personal Protective Equipment (PPE).
Work safely by not causing unsafe conditions or doing unsafe acts.

Lean: Support and contribute actively in Lean sigma programs and activities towards delivery of the set target.
Switch off the machinery if it is not operating; or Switch off the lights and air conditioning if you are the last person to leave the premise.
Simplify processes and improvements; reduce printing or photocopying; use recycle papers.

Basic Qualifications:
Graduate in science/Engineering with minimum 1-year experience in QC in any industry

Preferred Knowledge, Skills and Abilities:
Graduate in science/Engineering with minimum 1-year experience in QC in any industry.
Knowledge in QC
Knowledge in calibration activities.
Good written and communication skills in English.
Good interpersonal skills

Travel Requirements:
Must be able to travel up to 10% of the time.

Physical & Mental Requirements:
Physically fit & Healthy

Competencies/Authorities
Knowledge in Documentation and GLP, GDP & GMP
Knowledge in Computer

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status. If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com. Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

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