×
Register Here to Apply for Jobs or Post Jobs. X

Sr. Specialist HPLC​/Lab Manager QC

Job in Fremont, Alameda County, California, 94537, USA
Listing for: Asahi Kasei Corporation
Full Time position
Listed on 2026-08-31
Job specializations:
  • Quality Assurance - QA/QC
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 140000 - 170000 USD Yearly USD 140000.00 170000.00 YEAR
Job Description & How to Apply Below
Position: Sr. Specialist HPLC / Lab Manager QC

The Asahi Kasei Group operates with a commitment of creating for tomorrow. Our business sectors, Material, Homes, and Health Care, contribute to the development of society by anticipating the changing needs of those around the world. We look for candidates that offer a fresh perspective and a variety of skills to help us achieve our commitment. Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes.

Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients’ expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.

Bionova became a subsidiary of Asahi Kasei Medical in May 2022, a division of Tokyo-based Asahi Kasei Group. This acquisition has enabled Bionova to greatly accelerate growth of the business, both in capacity of current service offerings and expansion into new service offerings.

Company:
Bionova Scientific LLC

Location:

Fremont, CA

Job Description

Partnering closely with the Senior Director of Quality Control, the Sr. Specialist HPLC / Lab Manager QC will help support the establishing efficient, compliant, and high-performing laboratory operations with a focus on HPLC and CE in a regulated GMP environment. This role requires deep expertise in all aspects of HPLC testing and a sound understanding in CDS software, preferably Empower, Quality Control GMP operations and quality systems, along with demonstrated leadership capability and the ability to effectively influence teams and stakeholders across organizational and global environments.

Position

Responsibilities
  • Serve as an HPLC subject matter expert and drive improvement of HPLC workflows and our Empower based CDS.
  • Author and maintain analytical methods, validation and qualification documentation, and relevant laboratory procedures.
  • Authoring analytical procedures and their associated validation and qualification documents for new analytical testing methods or equipment or training and mentoring junior QC team members therein
  • Support troubleshooting and transfer tests from Analytical Development into GMP operations.
  • Review and interpret analytical data to identify trends, assess risk, and initiate appropriate corrective actions.
  • Lead investigations for deviations, including OOS, OOT, OOR, and OOE, performing root cause analysis and defining corrective and preventive actions.
  • Act as a subject matter expert during client audits and regulatory inspections, representing QC analytical and operational processes.
  • Implement Lean laboratory practices and drive continuous improvement to enhance efficiency and performance.
  • Support cross-functional QC activities by providing cross-trained resources to address urgent analytical needs.
  • Lead, coach, and develop a team of analysts to ensure high technical and performance standards.
  • Establish and maintain compliant laboratory operations aligned with Bionova quality standards and regulatory requirements, including the definition and monitoring of key performance indicators.
Working Conditions

This position requires work in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.

Qualifications
  • Bachelor of Science degree or equivalent in a scientific field
  • Minimum of 4 years of experience in analytical or quality control environments.
  • Minimum of 2 years of GMP Quality Control Laboratory.
  • Strong working knowledge of HPLC and CE analytics with expertise in method development and GMP validation.
  • Experience in designing CDS workflows (data review, audit trails, design of workflows, custom fields…)
  • Expertise in data analysis, trend analysis, and statistical methods.
  • Excellent written and verbal communication skills to effectively document findings and present technical information.
  • Working…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary