Bachem

QMS Process Engineer

Bachem$82K — $141K *
Vista, CA 92084In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in scientific or technical discipline (chemistry, biotechnology, engineering, life sciences)
  • Master's Degree preferred
  • 5+ years' experience in Quality Assurance within a cGMP Manufacturing environment
  • 2+ years' project management experience preferred
  • Excellent written and oral communication skills, with experience in writing SOPs and process mapping
  • Knowledge of electronic software used in quality systems (e.g., Veeva, MasterControl, LIMS, SAP)
  • Detail-oriented with project management capabilities and the ability to thrive in a fast-paced environment

Responsibilities

  • Manage projects for QMS enhancement and collaborate with local and global teams
  • Assist in improving metrics and reporting on the health of the US quality system
  • Draft and review GMP documentation, including SOPs and protocols
  • Identify harmonization and optimization opportunities within global GMP practices
  • Implement improvements in quality systems while considering LEAN GMP approaches
  • Resolve issues with GMP electronic systems and support effective implementation
  • Collaborate with QA and other departments to enhance QMS processes and documentation
  • Support GMP audits and provide compliance guidance as needed

Benefits

  • Competitive pay
  • Annual performance bonus
  • Comprehensive Medical/Dental/Vision coverage
  • 401(k) plan with employer contribution
  • Paid vacation, personal, and sick days
Full Job Description
A brief overview

The Quality Management Systems (QMS) Process Engineer / Sr. Process Engineer plays a critical role within the Quality Systems and Compliance team. This position is responsible for supporting the ongoing development, maintenance, and oversight of a new electronic QMS, along with transitioning from the existing EQMS, and associated Quality system processes across Bachem's U.S. sites, while also partnering with QA and other stakeholders at European locations. Additionally, the incumbent serves as a subject matter expert in electronic quality systems implementation, including but not limited to Veeva, MasterControl, LIMS, and SAP.

Expected duration: This is a fulltime salaried position with full benefits. The role is primarily dedicated to supporting a quality system migration project with an anticipated duration of two years. It is expected the role will transition into the larger quality organization upon completion of project.

What you will do

  • Manage QMS system enhancement projects and collaborate locally and globally with the continuous improvement, maintenance, and oversight of the Quality Systems.
  • Assist with Improving metrics/calculations and issuing reports to assess the health of Bachem US quality system including Global level reporting and assessment.
  • Process mapping, Draft, and review of GMP documentation e.g. SOPs, protocols, reports
  • Proactively develop, identifying harmonization potential and optimization of global GMP concept and quality practices within the Bachem Quality Assurance organization within the US and across international sites.
  • Suggest and implement improvements in quality systems, policies, and SOPs taking into account LEAN GMP approaches to optimize and improve existing processes in quality.
  • Resolve problems with GMP electronic systems and provide guidance on EQMS topics, providing hands-on support for local sites for the effective and lean implementation of these GMP processes and concepts
  • Collaborate with QA team members and with other departments to implement improved QMS processes, systems quality culture and documentation landscape.
  • Support GMP audits for internal operations, GMP compliance improvements and provide GMP compliance guidance to other departments and BAM Sites as needed.


Qualifications

  • Bachelor's Degree in scientific or technical discipline (chemistry, biotechnology, engineering, life sciences)
  • Master's Degree Master's Degree (preferred)
  • 5+ years' experience in Quality Assurance with a cGMP Manufacturing organization
  • 2+ years' project management experience (preferred)
  • Excellent written and oral communication skills and experience in writing standard operating procedures (SOP), and process mapping
  • Experience with supporting/conducting audits and developing quality system metrics
  • Comprehensive knowledge of electronic software used in quality systems (e.g. Veeva MasterControl, LIMS, SAP etc.)
  • Ability to manage projects, organize and work in a fast-paced 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 problems
  • Ability to work in a team environment and interact well with co-workers, customers, regulatory agency auditors and senior management
  • Hands-on experience with electronic system configuration (preferred)


Base Annual Salary Ranges:

Engineer: $82,969 - $114,083

Sr. Engineer: $103,104 - $141,768

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.

Share this job posting by email

About Bachem

Bachem is a Swiss biochemical company that provides services to the pharmaceutical and biotechnology industries. The company specializes in the development of innovative, efficient manufacturing processes and the reliable production of peptide-based active pharmaceutical ingredients. Bachem has a global presence with headquarters in Switzerland and subsidiaries in Europe, the US, and Asia. The company was founded in 1971 and has since become a leading supplier of peptides worldwide. Bachem's products are used in the treatment of diseases such as diabetes, cancer, and cardiovascular diseases.
Learn more about Bachem
Size
1,200 employees
Industry

Similar Jobs

More Jobs at Bachem

More Pharmaceuticals & Biotech Jobs

Find similar QMS Process Engineer jobs: