Posted:3 hours ago|
Platform:
Work from Office
Full Time
Use Your Power for Purpose
Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, which is both science and risk-based, is designed to be flexible, innovative, and customer-oriented. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contribution is crucial and will have a direct impact on patients.
What You Will Achieve
In this role, you will:
Investigate quality issues within manufacturing.
Examine deviations, and atypical investigations
Identify root causes and suggest effective corrective action plans
Ensure all reports comply with regulatory requirements and company policies
Contribute to moderately complex projects, managing your own time to meet targets
Develop plans for short-term work activities within a collaborative team environment
Apply skills and discipline knowledge to contribute to work within the Work Team
Make decisions to resolve moderately complex problems in standard situations
Work under general supervision, following established procedures and general instructions
Periodically review work, and may review the work of other colleagues in a mentor role
Here Is What You Need (Minimum Requirements)
BA/BS with at least 2 years of experience or MBA/MS with any years of experience or associates degree with at least 6 years of experience or high school diploma (or equivalent) with at least 8 years of relevant experience
Proven record of problem-solving and decision-making skills
Experience in the pharmaceutical industry
Strong background and knowledge in manufacturing, compliance, and technology investigations, processes, and systems
Ability to work both independently and collaboratively
Effective communication skills, both written and verbal
Computer literate with superior skills in managing Excel spreadsheets
Bonus Points If You Have (Preferred Requirements)
Masters degree
Experience with investigations, including conducting and writing investigations using methodology
Familiarity with regulatory requirements and quality standards
Strong analytical and critical thinking skills
Ability to manage multiple projects simultaneously
Experience with root cause analysis and corrective action plans
Excellent organizational skills
Ability to mentor and guide junior colleagues
Strong interpersonal skills and the ability to foster a collaborative team environment
Quality Assurance and Control
Pfizer
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.
We have sent an OTP to your contact. Please enter it below to verify.
Instantly access job listings, apply easily, and track applications.
visakhapatnam
4.0 - 8.0 Lacs P.A.
Salary: Not disclosed
visakhapatnam, andhra pradesh, india
Salary: Not disclosed
visakhapatnam
3.6 - 7.5 Lacs P.A.
pendurthi, andhra pradesh, india
Salary: Not disclosed
visakhapatnam, andhra pradesh, india
Salary: Not disclosed
tirunelveli, tiruchirapalli, coimbatore
Experience: Not specified
3.0 - 3.5 Lacs P.A.
kolkata, mumbai, new delhi, hyderabad, pune, chennai, bengaluru
Experience: Not specified
1.0 - 4.0 Lacs P.A.
2.0 - 6.0 Lacs P.A.
2.0 - 4.0 Lacs P.A.
