Sr. QC Associate, Analytical
Company: Wacker Chemie AG
Location: San Diego
Posted on: May 9, 2025
Job Description:
Press Tab to Move to Skip to Content LinkSelect how often (in
days) to receive an alert:Date: May 2, 2025Do you want to take
responsibility and make a difference with your work? With your
expertise, we can achieve great goals together. We are WACKER -
Reliable. Determined. Ambitious. As one of the world's most
research-intensive chemical companies, we've been making countless
products that are an integral part of your everyday life possible
for over 100 years. From vegan food to resource-efficient buildings
to solar cells, we develop sustainable solutions that change the
future.we are looking for you as a(n) Sr. QC Associate,
Analytical.The Senior QC Associate (Analytical) is experienced with
a wide variety of analytical techniques, international regulations,
and method development and validation. This role will lead method
transfer, development, and qualification projects. This role is
proficient at summarizing data and presenting it to internal and
external parties. This role works closely with people at Wacker
Biotech USA, our sister sites, and clients, to ensure project
commitments are met in a timely manner. This position will mentor
other quality associates to support technical transfers, method
validation, and quality investigations. This position requires
hands-on laboratory work and close collaboration with the QC
control team, Process Development Team, and the Operations team,
and external clients. This position is expected to be highly
knowledgeable of relevant cGMP guidelines, ICH Guidance, and other
regulatory considerations.Essential Functions:
- Perform routine, non-routine and complex analytical testing
with independently.
- Develop, qualify, and validate complex analytical test methods
following international guidance's, and client requirements
independently.
- Leads QC initiatives. Develop and implement improvement
projects seeking input from affected departments / parties as
needed.
- Mentors' other quality control analysts. Ensures personnel
understand various analytical assays and standard operation
procedures as well as conform to any departmental procedures.
- Perform routine laboratory maintenance including, monthly
routine cleaning procedures to ensure safety of laboratory
personnel as well as monitor disposable equipment and reagent
supplies to make certain materials are available for use.
- Prioritize daily tasks, related to operations, technology
transfers, analytical testing and validation including equipment
and procedures.
- Document and investigate any out of specification results,
deviations, or investigations independently. Assist in resolving
any out of specification and out of trending results as well as
performing and developing any corrective and preventative
measures.
- Develop and revise SOPs under data integrity guidelines as well
as perform periodic revisions to ensure the procedures are up to
date to current standards.
- Assist Quality Assurance in ensuring compliance with applicable
quality standards and regulatory requirements.Position
Qualifications:
- Bachelor, Masters, or PhD of Science Degree in the Biological
Sciences, Bioengineering or Chemistry with a combination of
education and experience performing biochemistry, molecular
biology, microbiology, and chemistry.
- 8+ years relevant experience with BS; 6+ years relevant
experience with MS; 0+ years relevant experience with PhD
- Ability to travel up to but not limited to 5%.
- The Sr. QC Associate must be accountable for the work
performed, productive within the company, provide open
communication, and exemplify effective teamwork skills.
- The Sr. QC Associate must be capable of being highly
independent, and able to accomplish tasks with minimal input.
- The Sr. QC Associate must be capable of mentoring other quality
professionals and working closely with other departments.
- The position is responsible for performing and demonstrating
the highest form of quality in the pharmaceutical industry,
understanding the cGMP regulations, and implementing these
practices on the work being performed.
- Knowledgeable using Microsoft Office as well as developing any
documentation and creating tables for laboratory inventory and data
entry.
- Highly organized, detail oriented, with excellent record
keeping skills.
- Sound scientific judgement with good communication skills and
the ability to work effectively with others.The anticipated salary
range for candidates who will work in California is $110K - $140K.
The final salary offered to a successful candidate will be
dependent on several factors that may include but are not limited
to the type and length of experience within the job, type and
length of experience within the industry, education, etc. Wacker is
a multi-state employer, and this salary range may not reflect
positions that work in other statesWhat do we offer?WACKER is an
equal opportunity employer committed to diversity, equity,
inclusion, and sustainability. We are innovators, researchers, and
pioneers and we believe that our individual differences are our
collective strength. We foster an inclusive environment that
promotes individuality, celebrates diversity, and builds cohesive
teams. Together, we create exceptional value for our employees, our
customers, and our communities by creating a culture of inclusion
and equity that enables, empowers, and values our diverse
contributions.WACKER strives to reward its employees in a fair and
equitable manner. Our Total Rewards Package considers employee
wellbeing and is comprised of compensation, benefits, work-life
balance, performance & recognition, and career
development.Compensation and Incentive plansMedical, Dental, and
Vision Insurance effective day 1Paid Time Off in addition to
personal days and holidaysPaid parental leaveFlexible hybrid work
arrangements401(k) with company matchEducation Assistance
ProgramCareer development and advancement opportunitiesSupport for
Community InvolvementWe are looking forward to your online
application at www.wacker.com.
Reference Code:29373The information contained herein is not
intended to be an all-inclusive list of the duties and
responsibilities of the job, nor are they intended to be an
all-inclusive list of the skills and abilities required to do the
job.A minimum requirement for this US-based position is the ability
to work legally in the United States on a permanent unrestricted
basis. Visa sponsorship is not available for this position,
including for any type of US permanent residency (e.g., for a green
card).WACKER is proud to be an Equal Opportunity/Affirmative Action
Employer, making decisions without regard to race, color, religion,
creed, sex, sexual orientation, gender identity, marital status,
national origin, age, veteran status, disability, or any other
protected class.
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Keywords: Wacker Chemie AG, Lake Elsinore , Sr. QC Associate, Analytical, Other , San Diego, California
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