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Quality Assurance Specialist
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Quality Assurance Sp....
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Quality Assurance Specialist

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1 Vacancy
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Jobs by Experience

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2-3years

Job Location

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Pasadena - USA

Monthly Salary

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Not Disclosed

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Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Req ID : 2843077

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.

Our goal is to skyrocket our clients success and you can be a part of our team s achievements. Employing a global team of skilled professionals and experts that span across strategically located offices in North America Europe Asia and the Middle East we are proud of the roles we have fulfilled to help our clients achieve success.


The Experience


With operations spanning the globe and featuring a multicultural team PSC Biotech is passionate about bringing the best and brightest together in an effort 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 firm believers in coaching and developing the next generation of industry leaders and influencers. As such you will not only be offered compensation and benefits structure that rewards you but also be provided with the tools that will help you grow and learn.


At PSC Biotech it s about more than just a job it s about your career and your future.


Your Role


We are hiring a Quality Assurance Specialist to facilitate document control including document changes and change control document review and QMS maintenance.


  • Support the review approval distribution and timely processing of required quality documentation.
  • Coordinate the processing of new documentation document updates and changes.
  • Monitor document change control processes ensuring that all changes are properly documented reviewed and approved.
  • Collaborate with cross functional teams to ensure that documentation is accurate and maintained in accordance with established standards and guidelines.
  • Work closely with document owners and change owners in order to ensure any deficiencies are addressed and resolved.
  • Provide thorough review of internal documents to ensure alignment with internal standards.
  • Identify and address any nonconformances or gaps in document control processes.
  • Maintain QMS record storage.
  • Prepare documents and records for required transfer activities.
  • Identify opportunities for process improvements within the document control function driving efficiencies and enhancing effectiveness.
  • Regularly review document control procedures and systems recommending and implementing enhancements as necessary.
  • Communicate changes to document control processes and requirements effectively to relevant stakeholders.
  • Additional responsibilities as required.

Requirements

  • Degree in relevant field.
  • 23 years experience of document control and change control management within the pharmaceutical medical device or biotech industries.
  • Strong computer skills including proficiency in Microsoft Office Suite. Highly skilled in Excel.
  • Strong knowledge of regulatory requirements (GMP ISO QSR etc.).
  • Familiar with document control management systems.
  • Familiar with CAD software and interpreting technical drawings.
  • Experienced with document indexing structures scanning and high volume printing.
  • Excellent communication skills both verbal and written.
  • Excellent organizational skills and attention to detail with the ability to manage multiple tasks and priorities effectively.
  • Ability to collaborate effectively with crossfunctional teams.
  • Analytical mindset with the ability to identify issues analyze and implement solutions.


Benefits

Offering a full suite of benefits PSC Biotech is firmly focused on diligently investing in our employees who enable our company to fulfill our mission and achieve success. We want to promote balance so you not only enjoy your work but also have the time and resources to live your life happy and healthy.

  • 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 Holidays
  • Education Assistance
  • Pet Insurance
  • Discounted rate at Anytime Fitness
  • Financial Perks and Discounts

Estimated pay (based on experience): $80000 $100000


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.



Degree in relevant field. 2-3 years experience of document control and change control management within the pharmaceutical, medical device, or biotech industries. Strong computer skills, including proficiency in Microsoft Office Suite. Highly skilled in Excel. Strong knowledge of regulatory requirements (GMP, ISO, QSR, etc.). Familiar with document control management systems. Familiar with CAD software and interpreting technical drawings. Experienced with document indexing structures, scanning, and high volume printing. Excellent communication skills both verbal and written. Excellent organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively. Ability to collaborate effectively with cross-functional teams. Analytical mindset with the ability to identify issues, analyze, and implement solutions.

Employment Type

Full Time

Company Industry

About Company

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