Job Overview
Compensation
Hourly
Range $30.01 - $41.27
Benefits
competitive pay
Annual performance bonus
Medical insurance
Dental Insurance
Vision Insurance
401K plan with employer contribution
Paid vacation
Personal Days
sick days
Job Description
Bachem Americas is a prominent leader in the pharmaceutical and biotech industry, specializing in the development and manufacturing of peptides and complex biochemicals. Known for its commitment to quality and innovation, Bachem operates with a strong focus on compliance with Good Manufacturing Practices (GMP) and sustainability. The company prides itself on a culture of continuous improvement, safety, environmental responsibility, and inclusiveness, supporting a diverse workforce where merit, skill, and qualifications drive career advancement. Bachem offers competitive compensation packages and comprehensive benefits to support its team members' professional and personal well-being.
The Quality Control Scientist role at Bachem Americas involves key responsibilities in laboratory day-to-day operations linked to quality assurance in the manufacturing of peptides. Reporting to the QC Director and Supervisor, the scientist plays a critical role in maintaining and enhancing GMP compliance through testing, documentation, and analysis. This position operates on a Monday to Friday schedule from 7:00 am to 3:30 pm, providing a stable work structure for candidates.
In this capacity, the Quality Control Scientist manages raw material, in-process, and final product testing to ensure that all materials meet stringent quality standards. The scientist collaborates with QC staff and other departments to create and revise control documents such as specifications, SOPs (Standard Operating Procedures), and STMs (Standard Test Methods). Maintaining and verifying the calibration and validation of QC analytical equipment like HPLC, UPLC, GC, Mass Spectrometry, UV spectroscopy, and others is a vital part of the role, guaranteeing accuracy and reliability in all testing activities.
Additionally, the position demands a proactive approach to problem-solving, including investigating deviations or out-of-specification results and supporting validation and stability studies for continuous quality improvement. The candidate must understand and adhere to safety guidelines specific to working with toxic chemicals and large volumes of substances used in peptide production environments.
Bachem emphasizes the importance of thorough documentation consistent with cGMP standards to uphold quality and regulatory compliance. The Quality Control Scientist is expected to be detail-oriented, organized, and an effective communicator, capable of working independently as well as within a team environment. The role offers an hourly wage range dependent on experience and education, with Scientist I earning between $30.01 and $41.27 per hour and Scientist II earning between $34.70 and $47.71 per hour. Placement within this range considers education levels, skill sets, prior experience, and training.
This opportunity is ideal for professionals with a Bachelor’s or Master’s degree in Chemistry or a related field and a minimum of three years of experience in a GMP-regulated pharmaceutical or biotech environment. Bachem also fosters a culture of corporate social responsibility, standing out with a Gold Medal recognition from EcoVadis for environmental stewardship and sustainable business practices, ensuring their impact on future generations is minimal. Joining Bachem means becoming a part of a forward-thinking, environmentally conscious company committed to excellence and inclusivity in the workplace.
The Quality Control Scientist role at Bachem Americas involves key responsibilities in laboratory day-to-day operations linked to quality assurance in the manufacturing of peptides. Reporting to the QC Director and Supervisor, the scientist plays a critical role in maintaining and enhancing GMP compliance through testing, documentation, and analysis. This position operates on a Monday to Friday schedule from 7:00 am to 3:30 pm, providing a stable work structure for candidates.
In this capacity, the Quality Control Scientist manages raw material, in-process, and final product testing to ensure that all materials meet stringent quality standards. The scientist collaborates with QC staff and other departments to create and revise control documents such as specifications, SOPs (Standard Operating Procedures), and STMs (Standard Test Methods). Maintaining and verifying the calibration and validation of QC analytical equipment like HPLC, UPLC, GC, Mass Spectrometry, UV spectroscopy, and others is a vital part of the role, guaranteeing accuracy and reliability in all testing activities.
Additionally, the position demands a proactive approach to problem-solving, including investigating deviations or out-of-specification results and supporting validation and stability studies for continuous quality improvement. The candidate must understand and adhere to safety guidelines specific to working with toxic chemicals and large volumes of substances used in peptide production environments.
Bachem emphasizes the importance of thorough documentation consistent with cGMP standards to uphold quality and regulatory compliance. The Quality Control Scientist is expected to be detail-oriented, organized, and an effective communicator, capable of working independently as well as within a team environment. The role offers an hourly wage range dependent on experience and education, with Scientist I earning between $30.01 and $41.27 per hour and Scientist II earning between $34.70 and $47.71 per hour. Placement within this range considers education levels, skill sets, prior experience, and training.
This opportunity is ideal for professionals with a Bachelor’s or Master’s degree in Chemistry or a related field and a minimum of three years of experience in a GMP-regulated pharmaceutical or biotech environment. Bachem also fosters a culture of corporate social responsibility, standing out with a Gold Medal recognition from EcoVadis for environmental stewardship and sustainable business practices, ensuring their impact on future generations is minimal. Joining Bachem means becoming a part of a forward-thinking, environmentally conscious company committed to excellence and inclusivity in the workplace.
Job Requirements
- bachelor's degree in chemistry or related field
- minimum of 3 years' experience in GMP pharma/biotech facility
- experience with equipment maintenance programs
- ability to use analytical techniques including GC, HPLC/UPLC, UV-spectrophotometer
- excellent written and oral communication skills
- basic computer knowledge including Microsoft Word, Excel and PowerPoint
- ability to work under pressure in a fast-paced environment
- detail oriented and ability to troubleshoot problems
- ability to work independently and manage time
- excellent organizational skills
- flexibility to work evenings and occasional weekends
Job Qualifications
- bachelor's degree in chemistry or related field
- master's degree in chemistry or related field preferred
- minimum of 3 years' experience in GMP pharma/biotech facility
- experience with equipment maintenance programs
- experience with analytical techniques and instruments including GC, HPLC/UPLC, UV-spectrophotometer
- 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 environment
- ability to communicate proactively and solution-focused
- detail oriented with problem-solving skills
- ability to work independently and manage time
- ability to communicate effectively and function well in a team environment
- ability to review Certificate of Analysis for reagents for the creation of specification documents
- strong organization skills to support document creation and approval
- flexibility to work some nights and occasional weekends based on business needs
Job Duties
- maintain and perform daily operations in coordination with the QC director/supervisor to include testing of raw material/peptide samples and prioritizing projects
- write and work with other QC staff and other departments in the creation and approval of control documents such as specifications, SOPs, STMs
- maintain and perform regular verification of the QC equipment for GMP compliance
- implement and maintain GMP procedures including following SOPs and STPs, and maintaining proper documentation
- test, review, and release raw material used in the manufacturing facility for GMP compliance
- receive, test and release final product peptide manufactured at Bachem
- test and release in-process control samples used in manufacturing for GMP compliance
- maintain cGMP quality level of work including training, documentation and procedural work
- write/revise specifications and perform analytical analysis reviewing data for completeness and accuracy
- write SOPs, STPs and other related GMP documentation
- perform QC analysis using HPLC, UPLC, water, mass spec, UV, GC, melting point, optical rotation, TLC and wet chemistry lab work
- control raw material including receiving, quarantine, testing and release
- investigate any deviation or out of specification related to QC work
- execute validations including QC analytical methods
- follow safety guidelines for handling and disposal of toxic and large volume chemicals
- support validation and stability including analytical work, documentation and GMP procedures
Job Criteria
Experience
Mid Level (3-7 years)
Job Location
Your Profile Is Visible To Hiring Managers Across OysterLink.
We'll match you with best jobs
Get job offers faster
Search For More Opportunities:
How Candidates Get Hired Faster
Apply to 2–3 similar roles
Complete profile & get best matches
Check new opportunities daily
