What are the responsibilities and job description for the QC Senior Scientist position at Catalent Pharma Solutions?
**QC Senior Scientist**
The shift is Monday-Friday 8:00am - 5:00pm
A Quality Control (QC) Scientist's primary duty is to provide quality control, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. Responsibilities include performing and reviewing testing during phases of production, providing technical peer review of testing data, writing/revising technical documents including laboratory procedures, protocols and technical reports, independently utilizing microbiological or analytical instrumentation such as HPLC, GC, UV, ICP-MS, FTIR, TOC, CE, ICE, Karl Fisher, , Plate Reader, performing testing using methodologies such as SDS-PAGE, , IEF, ELISA, PCR, and recognizing atypical/out of specification (OOS) results and perform investigation to determine root cause and implement corrective and preventive actions.
This is a permanent, full time position. It is a salaried role. The shift is Monday - Friday 8:00am - 5:00pm. **This position offers a sign on bonus and relocation.**
Catalent Biologics in Bloomington, Indiana is a state-of-the-art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better, healthier lives.?
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee**
**The Role**
Has complete knowledge of varied aspects or a single specialized aspect of a discipline and some knowledge of principles and concepts in other disciplines
Applies technical and functional knowledge to conduct experiments/research in assigned area
May act as a technical resource within own work group/project team
Works independently to solve problems of moderate scope
Actively participates, suggests solutions to problems
Competent at risk mitigation for function
**The Candidate**
Bachelor's degree in science field with 5-7 years of experience, including 2 years GMP experience or other regulated industry
Master's degree in science field with 2-4 years of experience, including 2 years GMP experience or regulated industry
PhD in science field with 3-5 years of experience, including 2 years GMP experience or regulated industry
Must be able to read and understand English-written job instructions and safety requirements.
**Why you should join Catalent**
Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
152 hours of paid time off annually 8 paid holidays
Competitive salary with yearly bonus potential
Community engagement and green initiatives
Generous 401K match and Paid Time Off accrual
Medical, dental and vision benefits effective day one of employment
Tuition Reimbursement
**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.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ([ Link removed ] - Click here to apply to QC Senior Scientist 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 [ Email address blocked ] - Click here to apply to QC Senior Scientist . 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 [ Email address blocked ] - Click here to apply to QC Senior Scientist for us to investigate with local authorities.
The shift is Monday-Friday 8:00am - 5:00pm
A Quality Control (QC) Scientist's primary duty is to provide quality control, in-process, finished products, stability, cleaning process, and analytical method validation testing according to SOPs, cGMPs and regulatory guidelines. Responsibilities include performing and reviewing testing during phases of production, providing technical peer review of testing data, writing/revising technical documents including laboratory procedures, protocols and technical reports, independently utilizing microbiological or analytical instrumentation such as HPLC, GC, UV, ICP-MS, FTIR, TOC, CE, ICE, Karl Fisher, , Plate Reader, performing testing using methodologies such as SDS-PAGE, , IEF, ELISA, PCR, and recognizing atypical/out of specification (OOS) results and perform investigation to determine root cause and implement corrective and preventive actions.
This is a permanent, full time position. It is a salaried role. The shift is Monday - Friday 8:00am - 5:00pm. **This position offers a sign on bonus and relocation.**
Catalent Biologics in Bloomington, Indiana is a state-of-the-art, GMP manufacturing facility, providing one million sq/ft of drug substance manufacturing, drug product manufacturing, and related pharmaceutical services. This award-winning facility helps customers accelerate biologic drug development programs and bring better treatments to help patients live better, healthier lives.?
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer and Catalent employee**
**The Role**
Has complete knowledge of varied aspects or a single specialized aspect of a discipline and some knowledge of principles and concepts in other disciplines
Applies technical and functional knowledge to conduct experiments/research in assigned area
May act as a technical resource within own work group/project team
Works independently to solve problems of moderate scope
Actively participates, suggests solutions to problems
Competent at risk mitigation for function
**The Candidate**
Bachelor's degree in science field with 5-7 years of experience, including 2 years GMP experience or other regulated industry
Master's degree in science field with 2-4 years of experience, including 2 years GMP experience or regulated industry
PhD in science field with 3-5 years of experience, including 2 years GMP experience or regulated industry
Must be able to read and understand English-written job instructions and safety requirements.
**Why you should join Catalent**
Defined career path and annual performance review and feedback process
Diverse, inclusive culture
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives
152 hours of paid time off annually 8 paid holidays
Competitive salary with yearly bonus potential
Community engagement and green initiatives
Generous 401K match and Paid Time Off accrual
Medical, dental and vision benefits effective day one of employment
Tuition Reimbursement
**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.
Catalent is committed to the health and safety of its employees, visitors and the customers and patients we serve. As a result of the global pandemic, we have modified many of our recruitment and on-boarding processes to maintain everyone's safety. The Human Resources teams will communicate all necessary safety processes and procedures throughout each stage.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ([ Link removed ] - Click here to apply to QC Senior Scientist 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 [ Email address blocked ] - Click here to apply to QC Senior Scientist . 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 [ Email address blocked ] - Click here to apply to QC Senior Scientist for us to investigate with local authorities.
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