Ensure technical support for clinical and commercial products through technology transfer, process monitoring, troubleshooting, product stewardship, validation support, lifecycle management, and manufacturing readiness activities.
Lead technology transfer activities, including internal transfers and transfers from client sites, ensuring effective planning, risk assessment, process understanding, validation readiness, and technical documentation.
Lead efforts to improve manufacturing efficiency and process robustness through troubleshooting, root cause investigations, change controls, CAPAs, data analysis, and process optimization initiatives.
Serve as a member of the site leadership team, representing Technical Operations in site initiatives, operational readiness activities, and alignment with global technical standards.
Lead technical support for manufacturing activities, new product introductions, process improvements, and site operational initiatives in partnership with Manufacturing, Quality, Engineering, Supply Chain, R&D, and Project Management.
Support the development and implementation of technical capabilities, automation and digitalization initiatives, and platform technologies aligned with site and business needs.
Coach, develop, and retain technical talent by promoting knowledge sharing, continuous improvement, accountability, and professional development.
Partner with cross-functional stakeholders to support technical strategies, risk management activities, technology transfer execution, operational excellence initiatives, and COGS improvement efforts.
Support regulatory inspections, audits, validation activities, and inspection readiness efforts by providing technical expertise and documentation support.
Promote process safety, technical stewardship, and compliance with company policies, procedures, and GMP requirements.
Qualifications
Bachelor's Degree in Chemical Engineering, Biochemical Engineering, Pharmaceutical Sciences, Chemistry, or a related scientific or engineering discipline with equivalent relevant experience or
Master's Degree in Chemical Engineering, Biochemical Engineering, Pharmaceutical Sciences, Chemistry, or a related scientific or engineering discipline
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8+ years of GMP experience in pharmaceutical, biotech, CDMO, process development, manufacturing science, technical operations, or manufacturing environments with exposure to clinical and commercial manufacturing.
3+ years of leadership experience in Technical Operations, manufacturing science, process development, or related technical functions, including leadership of technical and cross-functional teams, technology transfers, process optimization, validation support, technical documentation, and lifecycle management activities.
Strong knowledge of GMP, quality systems, regulatory requirements, validation principles, process safety, and inspection readiness expectations.
Strong analytical, troubleshooting, decision-making, and problem-solving skills; familiarity with Lean Six Sigma and operational excellence methodologies.
Ability to lead and develop technical teams and effectively collaborate with cross-functional stakeholders.
Strong project management and communication skills with the ability to influence stakeholders and drive execution.
Understanding of budgeting, resource planning, COGS improvement opportunities, and business considerations that impact Technical Operations.
Ability to work effectively within a matrix organization and collaborate across multiple functions and sites.
Demonstrated ability to lead change, improve processes, and support implementation of new technologies and digital tools.
Placement of new hires in these wage ranges is based on several factors including education, skill sets, experience, and training.
Total Rewards
We offer all Team Members a total rewards package including competitive pay, annual performance bonus, a generous benefit package with comprehensive Medical/Dental/Vision coverage, 401(k) plan with employer contribution, and paid vacation, personal and sick days.
Corporate Social Responsibility
Bachem takes responsibility for future generations by a careful handling of resources and avoiding environmental risks. We continually improve our ecological performance and develop and implement new approaches for enhancing employees’ environmental awareness. EcoVadis has awarded Bachem Gold Medal status in their assessment of Bachem.
Bachem Americas is an Equal Opportunity Employer
As an equal opportunity employer, we celebrate the diversity of our team and are committed to building an inclusive workplace where individuals are hired and advanced based on merit, skills, and qualifications. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status, or other legally protected status.
At Bachem, you’ll find a diverse, multicultural team. The (a) in the job title stands for all. We welcome applications from all candidates. What matters are your skills and motivation—regardless of age, gender, background, religion, or sexual orientation.
Please note: unsolicited resumes from recruitment agencies will not be considered.
About Bachem
Pharmaceuticals & Biotech1,001-5,000Founded 1971
Bachem is a Swiss contract development and manufacturing organization (CDMO) specializing in peptides and oligonucleotides for pharmaceutical and biotechnology companies. Founded in 1971 and headquartered in Bubendorf, it supports research, clinical development, and commercial applications through sites in Europe, the United States, and Asia.
