Bachem

Process Engineer II

Bachem$83K — $114K *
Vista, CA 92084In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in life sciences or engineering; Master's preferred
  • 5+ years in pharmaceutical engineering/manufacturing
  • Strong grasp of engineering fundamentals and cGMP
  • Proficient in troubleshooting complex systems
  • Experience with USP/DSP processes and large-scale equipment
  • Preferred knowledge of automation systems like DeltaV and FactoryTalk

Responsibilities

  • Maintain USP/DSP equipment to minimize manufacturing downtime
  • Design and qualify batch processing and support systems
  • Troubleshoot automation systems and program recipes
  • Support CAPEX projects for efficiency improvements
  • Oversee commissioning and qualification of facilities and equipment
  • Maximize production success by reducing errors and failures
  • Communicate operational updates to management effectively

Benefits

  • Comprehensive Medical/Dental/Vision coverage
  • 401(k) plan with employer contribution
  • Paid vacation, personal and sick days
  • Annual performance bonus
  • Commitment to corporate social responsibility and environmental awareness
Full Job Description
A brief overview

The Process Engineer II is responsible for supporting, maintaining, and optimizing large-scale upstream and downstream production equipment and instrumentation to ensure reliable, continuous manufacturing operations with minimal downtime. Leveraging strong process mapping and analytical skills, this role leads the development and execution of process improvement initiatives, conducts engineering design evaluations, and identifies opportunities to enhance efficiency and product quality across USP/DSP processes.

In addition, the Process Engineer II evaluates equipment needs, researches potential solutions, and provides informed recommendations to management. The role also partners closely with third-party contractors to ensure timely completion of IQ/OQ/PQ activities. Strong independent troubleshooting capabilities are essential.

What you will do

  • Maintain all USP/DSP equipment and instruments at the ready-to-run status to ensure that manufacturing is continuously in operation with minimal downtime
  • When needed, be responsible for design, installation, and qualification of batch processing tanks, solvent recovery system, filter dryers, filtration system, ultra-low freezers, HVAC, solvent distribution and recovery system, compressed air, purified water, and wastewater system
  • Ability to learn the automation system trouble shooting including a programed recipe fixing, changing and testing.
  • Support production on CAPEX projects for production facility and equipment improvements in order to increase production efficiency and reduce cost
  • Perform activities associated with the design and qualification of the new and existing USP/DSP equipment used in a manufacturing plant
  • Support large-scale production process development and optimization projects
  • Provide technical guidance and support investigations for process related deviations, change control and operational excellence projects
  • Oversee implementation, commissioning, and qualification of USP/DSP facility and process equipment
  • Maximize the success rate for production operations by instituting programs to minimize human error, mechanical failure, contaminations, and procedural error
  • Maintain a safety-first approach in the large-scale manufacturing workplace
  • Communicate operational status regularly to senior management and corporate management, as required and appropriate. Communications include written documents and formal / informal oral presentations
  • Maintain a high level of compliance and efficiency to drive the organization to world-class manufacturing standards
  • Create new process and equipment drawings to existing processes based on specifications and standards
  • Update and maintain drawings and P&ID to reflect changes to existing processes
  • Responsible for trouble shooting and providing corrective action directives
  • Troubleshoot process equipment and ensuring that equipment works to its specifications and appropriate capacities
  • Create, execute validation protocols and write validation summary reports
  • Draft of new procedures, SOP's and protocols as well as training of staff for these expectations
  • Write technical reports to support the process development data.
  • Write standard operations procedures, standard test procedures, master batch records, and other related GMP documents.


Qualifications

  • Bachelor's degree in a life sciences or engineering field
  • Master's degree (preferred)
  • Minimum 5 years of experience of pharmaceutical engineering and/or manufacturing
  • Thorough understanding of engineering fundamentals
  • Deep knowledge of cGMP, pharmaceutical manufacturing facility, large-scale equipment, and engineering principles
  • Good understanding of computer programming and software development
  • Ability to troubleshoot equipment problems and perform complex system tests.
  • Technical knowledge of USP/DSP processes / equipment / automation / utilities (e.g. large-scale chemical reactor, cleavage vessel, deprotection vessel, solvent delivery system, agitator, batches processing, tank, filtration, purified water system, heat exchanger, HVAC, etc.)
  • Equipment Qualification and Validation IQ /OQ / PQ and SOPs
  • Excellent written and oral communication skills
  • Ability to communicate in a proactive and solutions-focused manner, including keeping management aware of potential issues
  • Ability to work independently and manage one's time
  • Ability to schedule and host internal/external meetings and negotiate with vendors, contractors, and customers for the best interest of the production department. Excellent computer knowledge, including Microsoft Word and Excel
  • Communicate effectively and ability to function well in a team environment
  • Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment
  • Detail oriented with the ability to troubleshoot and resolve equipment and process problems and deviations
  • Strong analytical and problem-solving skills.
  • Proficient in reading schematics and diagrams as well as other written materials
  • High level of safety awareness.
  • Good background for Automation systems software, i.e. DeltaV and FactoryTalk, is preferred.
  • Creative thinking skills with detail orientation.
  • Excellent manual dexterity.


Base Annual Salary Range:

Engineer II: $83,089 - $114,247

Sr. Engineer: $102,331 - $140,705

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.

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 Process Engineer II jobs: