Invitae
Invitae

60 Invitae Qc Analyst Jobs Hiring Near You

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Devens, MA · On-site

$26.75 - $36/hr

Quality Control Analyst Location: Devens, MA Duration: 6 Months(extension up to 3 year) QC Operations Bioassay analyst needed. Work in a cGMP laboratory and manufacturing environment following ...

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 3 PM - 11:30 PM. * This position is 100% on-site in Winchester, Kentucky. Catalent's Winchester location is the ...

Quality Control Analyst

Holly Springs, NC · On-site

$20.75 - $28/hr

Job Title - Quality Control Analyst Length of Assignment - 12 months Shift/Schedule Details - Standard Business Hours, M-F, 8:00am-5:00pm (one 30-minute lunch break is required) Location - Holly ...

Quality Control Analyst

Holly Springs, NC

$20.75 - $28/hr

Job Title - Quality Control Analyst Length of Assignment - 12 months Shift/Schedule Details - Standard Business Hours, M-F, 8:00am-5:00pm (one 30-minute lunch break is required) Location - Holly ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

Quality Control Analyst

Winchester, KY · On-site

$20.75 - $27.75/hr

Quality Control Analyst Position Summary * Typical working hours are Monday-Friday 11 PM - 7:30 AM (begins Sunday night at 11 PM and goes through Friday morning at 7:30 AM) * This position is 100% on ...

QC Analyst

Orangeburg, NY · On-site

$21 - $23/hr

Job Title: QC Analyst Location: Orangeburg, NY Type: Contract Compensation: $21-$23/hour Work Model: Onsite - onsite Hours: 2:00 pm -10:30 pm Responsibilities * Perform analyses of Clinical Chemistry ...

Quality Control Analyst

Berkeley, CA · On-site

$29.75 - $40/hr

Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Biological Development Assay Development, Quality Control (BD AD-QC) Position summary: The purpose of this position is to ...

Quality Control Analyst

Berkeley, CA

$29.75 - $40/hr

Quality Control Analyst Duration: 12 Months Location: Berkeley, CA 94710 Biological Development Assay Development, Quality Control (BD AD-QC) Position summary: The purpose of this position is to ...

Showing results 41-60

Invitae Jobs Information

What is it like to work at Invitae?

Invitae is a company that prioritizes collaboration, innovation, and a patient-centric approach to genetic testing and diagnostics. The company's structure is organized into multidisciplinary teams that work together to develop and improve genetic testing products, with a focus on creating a supportive and inclusive work environment. Working at Invitae may appeal to candidates who are passionate about advancing genetic medicine and are interested in contributing to a mission-driven organization that aims to improve human health.

What makes Invitae an attractive place to work?

Invitae is a leading genetic information company that aims to make high-quality genetic testing accessible to everyone, positioning itself at the forefront of the rapidly evolving genetic medicine industry. The company's workplace is characterized by a culture of innovation, collaboration, and teamwork, with opportunities for employees to contribute to cutting-edge research and development in genetics and genomics. By joining Invitae, individuals can leverage their skills and expertise to drive meaningful impact in the field of genetic medicine and enjoy opportunities for professional growth and development.

What other companies are hiring for Qc Analyst jobs?

$20.75 - $27.75/hr

Full-time

Life, Retirement, PTO

Re-posted 7 days ago


Catalent rating

7.6

Company rating: 7.6 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

59th of 86 rated pharmaceutical


Job description

Quality Control Analyst

Position Summary

  • Typical working hours are Monday-Friday 11 PM - 7:30 AM (begins Sunday night at 11 PM and goes through Friday morning at 7:30 AM)

  • This position is 100% on-site in Winchester, Kentucky.

Catalent's Winchester location is the flagship US manufacturing location for large scale oral dose forms, with integrated analytical and development services. With 28 years of expertise in product development, technology transfers and commercial manufacturing, and roots in industry-leading Glatt technology.

The Quality Control Analyst performs the basic and critical experimental work of day-to-day analysis, including generation and analysis of data. The Quality Control Analyst works "hands on" in an analytical lab that requires analytical testing, computer operating, record keeping, and report writing abilities.

The Role

  • Performefficient/reliable/highqualityanalyticaltestinginaccordancewithUSP/NF/EP/JP/FCC/etc.orcustomer supplied guidelines. Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc.

  • Maintain accurate written records of all analysis performed.

  • Accurately interpret and effectively communicate analytical results and issues.

  • Schedule daily tasks in an organized and efficient manner.

  • Calibrate and maintain lab equipment and instrumentation.

  • Responsible for operating in a safe manner, must be familiar with basic laboratory and chemical hygiene practices

  • Perform peer review of analytical testing and write up. Write SOPs on an as needed basis.

  • Other duties as required in support of Catalent Pharma Solutions high performance

The Candidate

  • Bachelor's degree in a scientific field required (Chemistry or Biology preferred). Alternate degrees in a non-scientific field may be accepted with at least 2 years of relevant experience in a material testing laboratory.

  • 2+ years in Quality, Laboratory, Clinical, or Chemical manufacturing role preferred.

  • Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs. Operatingsafelyinadynamicenvironmentwhichincludesmobileandfixedequipmentandchanging conditions while completing job tasks that range from simple to complex and/or multi-tasking.

Why You Should Join Catalent

  • Several Employee Resource Groups focusing on D&I

  • Tuition Reimbursement- Let us help you finish your degree or earn a new one!

  • Generous 401K match

  • 152 hours accrued PTO + 8 paid holidays

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work.

Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers:

Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.


What Catalent employees say

Pay

Benefits

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Workplace

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About Catalent

Sourced by ZipRecruiter

Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Somerset, NJ, US

Year founded

2007

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