QA Computerized Systems Senior Specialist
Duchnice, PL
Boost your career with us
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
You will ensure that computerized systems supporting manufacturing, laboratory operations, and enterprise-level processes are compliant with applicable regulatory requirements (e.g. FDA 21 CFR Part 11, EU Annex 11). You will play a key role in the planning, execution, and documentation of validation activities.
Your key responsibilities:
- Define, plan, and report CSV activities in line with regulatory expectations.
- Review and approve validation documentation (e.g. URS, risk assessments, test protocols).
- Support CSV efforts across key areas: Production Systems, Laboratory Systems, and Enterprise Systems.
- Monitor validation project progress and escalate risks to ensure smooth implementation.
- Collaborate with system users, subject matter experts, and software vendors to implement validated solutions.
- Assess and define the appropriate level of validation required following system changes.
- Identify systems requiring validation using a risk-based approach.
- Represent the QA CSV function during internal and external audits.
- Train site personnel on CSV requirements and data integrity principles.
- Initiate and review quality actions in the TrackWise system (deviations, change controls, CAPAs).
- Continuously develop your knowledge in the areas of CSV and digital quality assurance.
Our expectations:
- Minimum 3 years of experience in the pharmaceutical, biotechnology, or related regulated industry.
- A degree in biotechnology, pharmacy, chemistry, engineering, or a related scientific/technical field.
- Strong understanding of cGxP requirements and data integrity principles.
- Proven experience in computerized systems validation (CSV), equipment qualification (production and lab), and quality documentation lifecycle
- management.
- Experience participating in audits and inspections, with the ability to present CSV topics to internal auditors and national/international
- regulatory authorities.
- Ability to work independently as well as effectively collaborate across departments.
- Excellent communication skills, decision-making ability, and time management.
What we offer:
- Competitive salary
- Private medical care
- Life insurance
- Employee Pension Plan (PPE)
- An extra vacation day
- and more..
Why you should work with us
Contact us
career@polpharmabiologics.com