Process Engineer
Process Engineer
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2-5years
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
PSC Biotech provides the life sciences with essential services to ensure that health care products are developed manufactured and distributed to the highest standards in compliance with all applicable regulatory requirements.
With operations spanning the globe and featuring a multicultural team PSC Biotech is passionate about bringing the best and brightest together to form something truly special. When you make the decision to join our team you will be offered the ability to feel inspired in your career explore your professional passions and work alongside a group of people who will value and nurture your talents.
We are currently seeking a Process Engineer with a background in pharmaceutical/biotech supporting the development of downstream process equipment operations.
You will work within a team of engineers and work closely with a crossfunctional team and coordinate activities between Manufacturing Quality and Validation. Working as part of a project team you will be required to carry out the development process engineering including creation of documentation.
Responsibilities:
- Execute activities and protocols required for separation unit operation development.
- Drafting finalization and approvals of protocols and final reports.
- SOP drafting finalization and approval.
- Troubleshoot and provide resolution to technical issues to support rampup and operations of equipment and facilities.
- Ability to interface with other departments to resolve issues related to equipment process and compliance.
- Complete relevant paperwork following GDP/GMP guidelines.
- Support process team projects and Continuous Improvement efforts.
- Share process knowledge with colleagues across shift.
- Manage sample coordination with Quality Control.
- Conduct Data analysis and analytical testing.
- Complete material assessments and meet/interface with external vendors (e.g. equipment suppliers).
Requirements
- Bachelor s degree in engineering or related field.
- 3 years or more of experience in a regulated industry including automation processes and facilities.
- Knowledge of technical validation and system documentation.
- Experience working in a GMP environment.
- Experience working in a cleanroom or laboratory environment preferred.
- Highly motivated and flexible and adaptable to a fastpaced and changing environment requiring effective interpersonal and teamwork skills.
- This position is 60%80% onsite (hybrid).
Benefits
- Medical Dental and Vision PSC pays 100% of all qualifying employee medical premiums and 50% for qualifying dependents.
- Insurance options for Employee Assistance Programs Basic Life Insurance Short/Long Term Disability and more.
- 401(k) and 401(k) matching.
- PTO Sick Time and Paid Holiday.
- Education Assistance.
- Pet Insurance.
- Discounted Fitness/Gym Rates.
- Financial Perks and Discounts.
Equal Opportunity Employment Statement:
PSC is committed to is committed to a policy of Equal Employment Opportunity with respect to all employees interns and applicants for employment. Consistent with this commitment our policy is to comply with all applicable federal state and local laws concerning employment discrimination. Accordingly the Company prohibits discrimination against qualified employees interns and applicants in all aspects of employment including but not limited to: recruitment interviewing hiring (or failure or refusal to hire) evaluation compensation promotion job assignment transfer demotion training leaves of absence layoff benefits use of facilities working conditions termination and employersponsored activities and programs including wellness social and recreational programs. Employment decisions will be made without regard to an applicant s employee s or intern s actual or perceived: race color religion sex (including pregnancy gender identity and sexual orientation) national origin age (40 or older) disability genetic information or any other status protected by law.
Bachelor s degree in engineering or related field. 3 years or more of experience in a regulated industry, including automation, processes, and facilities. Knowledge of technical validation and system documentation. Experience working in a GMP environment. Experience working in a cleanroom or laboratory environment preferred. Highly motivated and flexible, and adaptable to a fast-paced and changing environment, requiring effective interpersonal and teamwork skills. This position is 60%-80% onsite (hybrid)
Employment Type
Full Time
