Senior Manager GMP Quality Assurance
Senior Manager GMP Quality Assurance
Posted on :
20-01-2025
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1 Vacancy
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Monthly Salary
Not Disclosed
Salary Not Disclosed
Vacancy
1 Vacancy
Posted on :
20-01-2025
Job Description
Job Title: Senior Manager GMP Quality Assurance
Job Location: United States
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
Spyre Therapeutics is a clinicalstage biotechnology company that aims to create nextgeneration of inflammatory bowel disease (IBD) products by combining bestinclass antibody engineering rational therapeutic combinations and precision medicine approaches. Spyre's pipeline includes investigational extended halflife antibodies targeting α4β7 TL1A and IL23.
Role Summary
Spyre Therapeutics is seeking an exceptional Sr. Manager GMP Quality Assurance to join our Quality team. This individual will have the unique opportunity to assist the Sr. Director GMP QA in developing monitoring and maintaining all aspects of a quality system as it relates to cGMP requirements for a development and clinical phase organization pursuing multiple biologic monoclonal antibody candidates. This person will be responsible for Batch Release Change Control Qualifications Deviations and CAPAs as they relate to the CMOs and the production clinical drug substance and drug product. This role reports to the Sr. Director of GMP QA.
Key Responsibilities
As an equal opportunity employer Spyre is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race color religion national origin gender age sexual orientation physical or mental disability genetic information or characteristic gender identity and expression veteran status or other nonjobrelated characteristics or other prohibited grounds specified in applicable federal state and local laws. We also embrace differences in experience and background and welcome diversity of opinions and thought with active recruitment designed to create a stronger and better Spyre that is focused on developing lifechanging products for patients.
Spyre Therapeutics along with other biotech companies has become aware of a surge in email scams targeting prospective job candidates within our industry. Please be aware that official recruiters at Spyre Therapeutics only use email addresses with the domain “@spyre.com.” We want to also emphasize that we never request candidates to make any purchases or divulge sensitive personal information via email.
Please also be aware that all job postings will be listed on our website at spyre.com/careers/.
Role Summary
Spyre Therapeutics is seeking an exceptional Sr. Manager GMP Quality Assurance to join our Quality team. This individual will have the unique opportunity to assist the Sr. Director GMP QA in developing monitoring and maintaining all aspects of a quality system as it relates to cGMP requirements for a development and clinical phase organization pursuing multiple biologic monoclonal antibody candidates. This person will be responsible for Batch Release Change Control Qualifications Deviations and CAPAs as they relate to the CMOs and the production clinical drug substance and drug product. This role reports to the Sr. Director of GMP QA.
Key Responsibilities
- Manage and coordinate Quality Assurance related activities relating to the CMOs and TechOps teams as well as support the QA team in a regulated environment
- Support implementation of the Spyre Therapeutics’ quality strategy and culture
- Perform batch record review and product release activities to ensure all products released meet regulatory standards
- Assist with the creation of quality metrics related to the trending of nonconformance reports CAPAs and complaint investigations
- Review and approve master batch records analytical methods validation and cleaning protocols and reports standard operating procedures (SOPs) change control documents Quality Events etc. as needed
- Review Stability Protocols and resulting Data and Reports for compliance when required
- Work with Quality Operations to ensure compliance with the company’s corporate Quality Management System (QMS)
- Effectively collaborates with departments (i.e. Technical Operations CMC Regulatory and Clinical) on various projects/improvements when input/participation from Quality is needed
- Participate in specific Quality related projects in accordance with the company’s goals and business objectives
- Drive the spirit of teamwork across all functions by supporting a team approach with focus on our patients being the top priority
- Support regulatory authority inspections and partner audits
- Align daily actions with department goals and company culture
- Other duties as assigned
- Bachelor’s degree in a scientific discipline with 8 plus years in the Pharmaceutical/Biotechnology industry (an equivalent combination of education and experience may be considered)
- Proven ability to apply cGMP regulations 21 CFR Partand good documentation practices to daily activities governing the Spyre activities
- Clinical product batch release experience required; commercial product release is a plus
- Experience in investigations writing and review required
- Experience with third party testing vendors and quality control release assays is a plus
- Knowledge of a biologics manufacturing and fill/finish environment strongly preferred
- Detail oriented with strong written and verbal communication skills
- Ability to work independently with minimal direction within prescribed guidelines or as a team member
- Ability to work well in a deadlinedriven environment
- Travel may be required up to 15% of the time
- Opportunity to work in a fastpaced dynamic environment where you help shape the culture of our young company contribute broadly to advance meaningful medicines and learn quickly.
- Market competitive compensation and benefits package including base salary performance bonus equity grant opportunities health welfare & retirement benefits.
- Unlimited PTO
- Two oneweek companywide shutdowns each
- Commitment to provide professional development opportunities.
- Remote working environment with frequent inperson meetings to address complex problems and build relationships.
As an equal opportunity employer Spyre is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race color religion national origin gender age sexual orientation physical or mental disability genetic information or characteristic gender identity and expression veteran status or other nonjobrelated characteristics or other prohibited grounds specified in applicable federal state and local laws. We also embrace differences in experience and background and welcome diversity of opinions and thought with active recruitment designed to create a stronger and better Spyre that is focused on developing lifechanging products for patients.
Spyre Therapeutics along with other biotech companies has become aware of a surge in email scams targeting prospective job candidates within our industry. Please be aware that official recruiters at Spyre Therapeutics only use email addresses with the domain “@spyre.com.” We want to also emphasize that we never request candidates to make any purchases or divulge sensitive personal information via email.
Please also be aware that all job postings will be listed on our website at spyre.com/careers/.
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Employment Type
Full Time
Key Skills
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