Serán BioScience Jobs Hiring Now
Serán BioScience is hiring for 13 open roles on Migrate Mate as of July 16, 2026, concentrated in biotech & life sciences and engineering (Non-Software). Migrate Mate updates Serán BioScience's live openings daily. Serán BioScience is a contract pharmaceutical development and manufacturing organization specializing in drug product development, quality assurance, and laboratory services for life sciences clients.
Find Serán BioScience JobsOverview
Serán BioScience hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 13
- Top team
- Biotech & Life Sciences
- Seniority
- Mid to senior level
- Work type
- 8% remote or hybrid
- Top location
- Bend
Open Roles at Serán BioScience
Showing 13 of 13+ Serán BioScience jobs
Serán is seeking a QA Associate Director,who oversees the day-to-day operations of the Quality Assurance department with oversite of clinical manufacturing and warehouse activities in addition to disposition of raw materials and drug products. Required attributes include a results-driven and broad-minded quality assurance professional with extensive experience in compliance and regulations, quality systems management, investigations, training and mentoring, client relations, performance management, and change management. Extensive experience with direct or quality oversite of manufacturing operations is required.
The successful candidate will have excellent problem-solving skills and will identify critical quality objectives, develop cross-functional, collaborative, and creative teams, and improve, adapt, and execute practical solutions in competitive and fast-paced environments.Supervisory Responsibilities
- Leads and mentors Quality Assurance personnel.
- Recruits, interviews, hires and trains new staff.
- Oversees daily workflow of the department.
Responsibilities
- Leads and implements continuous improvement initiatives to reduce risk and improve efficiency for the company’s quality systems and department operations
- Management and scheduling of department operations
- Oversees and conducts review and approval of Investigations, CAPAs, Complaints, and Change Management
- Review and approval of SOPs, batch records, raw material records, and certificates of conformance/compliance
- Responsible for Quality oversight of activities involving raw material, drug product manufacturing, packaging, labeling, and warehouse activities
- Assures cGMP compliance systems and processes are in place to support raw material and drug product review, release, storage, and shipping
- Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first-time rate
- Supports internal audits, client audits and regulatory inspections
Required Skills and Experience
- Expert knowledge of GMP guidelines and Quality expectations for preclinical and clinical phase manufacturing operations
- In-depth understanding and application of cGMP principles, concepts, practices, and standards
- Experience with regulatory inspections by the FDA and EU authorities
- Ability to influence diverse stakeholders and drive accountability and decision-making cross functionally
- Demonstrated ability to partner with other functional groups to achieve business objectives
- Experience organizing and managing group responsibilities while working independently with minimal oversight
- Time and project management skills with the ability to multi-task and meet deadlines
- Excellent verbal and written communication skills
- Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company
- Excellent organizational skills and attention to detail
- Strong analytical and problem-solving skills
- Strong supervisory and leadership skills
Education and Experience
- Minimum of a bachelor’s degree, preferably in a scientific discipline. An advanced degree is preferred
- 10+ years previous GMP and Quality experience in the Pharmaceutical industry with quality oversite of Oral Solid Dose manufacturing
- Experience with regulatory inspections by the FDA and EU authorities
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Serán is seeking a QA Associate Director,who oversees the day-to-day operations of the Quality Assurance department with oversite of clinical manufacturing and warehouse activities in addition to disposition of raw materials and drug products. Required attributes include a results-driven and broad-minded quality assurance professional with extensive experience in compliance and regulations, quality systems management, investigations, training and mentoring, client relations, performance management, and change management. Extensive experience with direct or quality oversite of manufacturing operations is required.
The successful candidate will have excellent problem-solving skills and will identify critical quality objectives, develop cross-functional, collaborative, and creative teams, and improve, adapt, and execute practical solutions in competitive and fast-paced environments.Supervisory Responsibilities
- Leads and mentors Quality Assurance personnel.
- Recruits, interviews, hires and trains new staff.
- Oversees daily workflow of the department.
Responsibilities
- Leads and implements continuous improvement initiatives to reduce risk and improve efficiency for the company’s quality systems and department operations
- Management and scheduling of department operations
- Oversees and conducts review and approval of Investigations, CAPAs, Complaints, and Change Management
- Review and approval of SOPs, batch records, raw material records, and certificates of conformance/compliance
- Responsible for Quality oversight of activities involving raw material, drug product manufacturing, packaging, labeling, and warehouse activities
- Assures cGMP compliance systems and processes are in place to support raw material and drug product review, release, storage, and shipping
- Defines and maintains a strong people management, training, and engagement culture to ensure a high and constantly improving right first-time rate
- Supports internal audits, client audits and regulatory inspections
Required Skills and Experience
- Expert knowledge of GMP guidelines and Quality expectations for preclinical and clinical phase manufacturing operations
- In-depth understanding and application of cGMP principles, concepts, practices, and standards
- Experience with regulatory inspections by the FDA and EU authorities
- Ability to influence diverse stakeholders and drive accountability and decision-making cross functionally
- Demonstrated ability to partner with other functional groups to achieve business objectives
- Experience organizing and managing group responsibilities while working independently with minimal oversight
- Time and project management skills with the ability to multi-task and meet deadlines
- Excellent verbal and written communication skills
- Communicates effectively and maintains productive relationships with coworkers, clients, and other contacts outside of the company
- Excellent organizational skills and attention to detail
- Strong analytical and problem-solving skills
- Strong supervisory and leadership skills
Education and Experience
- Minimum of a bachelor’s degree, preferably in a scientific discipline. An advanced degree is preferred
- 10+ years previous GMP and Quality experience in the Pharmaceutical industry with quality oversite of Oral Solid Dose manufacturing
- Experience with regulatory inspections by the FDA and EU authorities
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Job Roles at Serán BioScience
Working at Serán BioScience
Serán BioScience's 13 open roles are mid to senior level, and about 8% are remote or hybrid. The most active teams are biotech & life sciences, engineering (Non-Software), and business operations. Serán BioScience is a contract development and manufacturing organization serving the pharmaceutical and biotechnology industries, providing services across formulation development, process development, quality control, quality assurance, and environmental monitoring. Most Serán BioScience roles are based in Bend.
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Browse jobs by roleSerán BioScience Jobs: Frequently Asked Questions
How many jobs is Serán BioScience hiring for right now?
Serán BioScience is hiring for 13 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in biotech & life sciences and engineering (Non-Software). Roles span scientific, quality, engineering, and business functions across the organization.
What kinds of roles does Serán BioScience hire for?
The most active teams are biotech & life sciences, engineering (Non-Software), and business operations. Serán BioScience regularly hires for pharmaceutical scientists, quality control and quality assurance professionals, process and laboratory engineers, environmental monitoring specialists, and business development positions. Most postings are mid to senior level, covering both individual contributor and leadership tracks within a contract development and manufacturing environment.
Are Serán BioScience jobs remote or in-person?
Mostly on-site. About 8% of Serán BioScience's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Bend. Each Serán BioScience listing shows its work location so you can filter before applying.
How do I apply to a job at Serán BioScience?
Find a role that fits your background among Serán BioScience's open listings on Migrate Mate, then follow the listing through to Serán BioScience's own careers page to submit your application directly. Serán BioScience manages its own hiring process, including interviews and offers, independent of Migrate Mate.
Does Serán BioScience hire entry-level?
Most of Serán BioScience's open roles on Migrate Mate are mid to senior level as of July 16, 2026. Entry-level openings are limited. Check individual Serán BioScience listings for stated experience requirements.
Where is Serán BioScience hiring?
Most Serán BioScience roles are based in Bend, and about 8% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.