Director, Production

Overview
Bachem is a leading, innovation‑driven company specializing in the development and manufacture of peptides and oligonucleotides. With over 50 years of experience and expertise Bachem provides products for research, clinical development and commercial application to pharmaceutical and biotechnology companies worldwide and offers a comprehensive range of services. Bachem operates internationally with headquarters in Switzerland and locations in Europe, the US and Asia. The company is listed on the SIX Swiss Exchange.

Responsibilities
Lead a team of production managers, chemists, and technicians in the day‑to‑day manufacturing of peptides and oligonucleotides.

Monitor production activities and adjust schedule to ensure on‑time delivery

Develop process improvements to optimize production speed and quality

Establish and enforce production and quality standards

Motivate team members to deliver exceptional work and exceed expectations

Organize job trainings for team members to achieve business objectives

Maintain all production‑related documentation for future reference purposes

Ensure that final product meets quality standards and customer specifications

Understand customer requirements and prepare production plan accordingly

Create, update and implement policies and procedures for manufacturing

Evaluate new equipment and technologies

Enroll cGMP guidelines

Maintain a clean and safe work environment by educating and directing personnel on the use of control points, equipment and resources

Maintain compliance with established safety policies and written procedures

Develop growth opportunities for employees

Maintain professional and technical knowledge by attending educational workshops, reviewing professional publications, benchmarking state‑of‑the‑art industry practices, and participating in professional societies

Ensure that reporting employees receive adequate environmental, health and safety training

Ensure that any operating or occupational accidents and incidents involving employees reporting to you are properly recorded and investigated to a productive conclusion. This includes ensuring employees are appropriately monitored and managed to address unacceptable levels of performance

Ensure a positive safety culture is developed within the area, and is supported by robust safety processes in accordance with industry standards and legislation

Ensure safety arrangements are adhered to and protect the health and safety of employees, visitors, contractors, and the public

Qualifications

PhD in Chemistry / Biological Chemistry / Chemical Engineering or related field with 5+ years relevant experience or

Master's Degree in Chemistry / Biological Chemistry / Chemical Engineering with 10+ years relevant experience or

Bachelor's Degree in Chemistry / Biological Chemistry / Chemical Engineering with 15+ years relevant experience

Experience managing large teams of 20+ people in a cGMP environment

Peptide and/or oligo nucleotide manufacturing experience in upstream or downstream manufacturing

Strong knowledge of chemistry, biological chemistry & chemical engineering along with cGMP manufacturing focus

Proficient with large scale manufacturing and process development

Proficient with various in‑process analytical methods

Excellent written and oral communication skills

Basic computer knowledge, including Microsoft Word, Excel and PowerPoint

Ability to effectively organize, multitask, and work in a fast‑paced, deadline driven work environment

Ability to communicate in a proactive and solution‑focused manner, including keeping management aware of potential issues

Detail oriented with the ability to troubleshoot and resolve technical and analytical problems

Ability to work independently and manage one’s time

Communicate effectively and ability to function well in a team environment

Base Salary Range
$129,992.80 - $162,491.00

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.

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.

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