Quality Control Analyst
Catalent · Winchester, KY · 1 mo ago
Quality AssuranceFull-time
We need to output HTML fragment with sections: Use for headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content.
We need to parse the job posting.
Key info:
- 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 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: Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer 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. Operating safely in a dynamic environment which includes mobile and fixed equipment and changing 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.
We need to remove boilerplate: EEO, accommodation notice, agency notice, security notice, California notice, volunteer work disclosure, Massachusetts lie detector test notice, etc.
Also remove application instructions (Visit Catalent Careers... maybe keep? It's not a specific instruction to apply; it's generic. Might be considered boilerplate. Safer to remove.
We need to include sections only if they have real specific content.
Potential sections:
- About the role: Could combine position summary and description of role. Might be "About the role" heading.
- Responsibilities: list of duties (perform testing, maintain records, interpret results, schedule tasks, calibrate equipment, safety, peer review, write SOPs, other duties). Use
for headings like About the role, Responsibilities, Requirements, Qualifications, Skills, Benefits, Pay, Schedule. Only include sections that have real specific content.
We need to parse the job posting.
Key info:
- 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 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: Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer 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. Operating safely in a dynamic environment which includes mobile and fixed equipment and changing 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.
We need to remove boilerplate: EEO, accommodation notice, agency notice, security notice, California notice, volunteer work disclosure, Massachusetts lie detector test notice, etc.
Also remove application instructions (Visit Catalent Careers... maybe keep? It's not a specific instruction to apply; it's generic. Might be considered boilerplate. Safer to remove.
We need to include sections only if they have real specific content.
Potential sections:
- About the role: Could combine position summary and description of role. Might be "About the role" heading.
- Responsibilities: list of duties (perform testing, maintain records, interpret results, schedule tasks, calibrate equipment, safety, peer review, write SOPs, other duties). Use - .
- Requirements / Qualifications: Bachelor's degree, alternate, 2+ years experience, lifting >50 lbs, operating safely, etc. Could be "Qualifications" or "Requirements". Use list.
- Skills: maybe not explicit; we could infer but better not to invent. Could skip Skills if not explicit.
- Benefits: Tuition reimbursement, generous 401K match, 152 hours accrued PTO + 8 paid holidays, Employee Resource Groups focusing on D&I. Also maybe "Catalent offers rewarding opportunities to further your career!" but that's vague. We'll include specific benefits.
- Pay: Not mentioned. So omit Pay section.
- Schedule: Typical working hours Monday-Friday 3 PM - 11:30 PM. That's schedule. So include Schedule section.
We also have location: 100% on-site in Winchester, Kentucky. Could be part of About the role or maybe a separate section? Not in list of headings; we could embed in About the role paragraph.
We must not repeat job title as heading.
We must not include Job ID/requisition numbers.
We must preserve all substantive information; do not invent or summarize away detail.
We need to output only HTML fragment, no /, no markdown fences.
Let's craft.
Structure:
About the role
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 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.
Responsibilities
- Perform efficient, reliable, high-quality analytical testing in accordance with USP/NF/EP/JP/FCC or customer-supplied guidelines.
- Typical testing may include dissolution, titration, polarimetry, loss on drying, viscosity, residue on ignition, heavy metal content, FTIR, HPLC, and GC.
- 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.
- Operate safely, 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.
Qualifications
- 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.
- Ability to assist with lifting of liquid containers and objects greater than 50 lbs.
- Ability to operate safely in a dynamic environment with mobile and fixed equipment and changing conditions while completing tasks ranging from simple to complex and/or multi‑tasking.
Benefits
- Several Employee Resource Groups focusing on diversity & inclusion.
- Tuition reimbursement – assistance to finish your degree or earn a new one.
- Generous 401K match.
- 152 hours accrued PTO plus 8 paid holidays.
Schedule
Typical working hours are Monday‑Friday, 3 PM – 11:30 PM.
We need to ensure we didn't duplicate schedule info (we already have in About the role). But we can keep schedule section with just the hours; the About the role also includes location and other details. It's okay to have some overlap? The instruction: Preserve ALL substantive information; do NOT invent or summarize away detail. It didn't forbid duplication, but better to avoid duplication. However schedule is already in About the role; we could remove schedule from About the role and keep only in Schedule section. But About the role also includes location and other details; we could keep schedule only in Schedule section and remove from About the role. Let's do that: About the role paragraph will not include schedule; we will put schedule in its own section.
Thus About the role paragraph: remove the schedule sentence.
Let's rewrite About the role:
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.
Schedule section: Typical working hours are Monday‑Friday, 3 PM – 11:30 PM.
Now ensure we didn't lose any other substantive info: The "Typical working hours are Monday-Friday 3 PM - 11:30 PM." is now only in Schedule section. Good.
Check other info: The "Catalent offers rewarding opportunities to further your career!" is vague; we omitted. The "Visit Catalent Careers to explore career opportunities." is boilerplate; omitted. The "personal initiative. dynamic pace. meaningful work." is vague; omitted.
Now ensure we didn't miss any specifics: The "Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs." we captured as ability to assist with lifting. Good.
"Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking." captured.
Now check if any other specifics: "The Role Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer supplied guidelines." captured.
"Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc." captured.
"Maintain accurate written records of all analysis performed." captured.
"Accurately interpret and effectively communicate analytical results and issues." captured.
"Schedule daily tasks in an organized and efficient manner." captured.
"Calibrate and maintain lab equipment and instrumentation." captured.
"Responsible for operating in a safe manner, must be familiar with basic laboratory and chemical hygiene practices" captured.
"Perform peer review of analytical testing and write up." captured.
"Write SOPs on an as needed basis." captured.
"Other duties as required in support of Catalent Pharma Solutions high performance" captured.
Now the "Why You Should Join Catalent" section: we captured benefits: Employee Resource Groups focusing on D&I, Tuition Reimbursement, Generous 401K match, 152 hours accrued PTO + 8 paid holidays. Also "Catalent offers rewarding opportunities to further your career!" we omitted as vague. Also "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." That's substantive but maybe could be included in About the role or Benefits? It's a selling point; maybe we could add a paragraph under About the role or a separate
About the role
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 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.
Responsibilities
- Perform efficient, reliable, high-quality analytical testing in accordance with USP/NF/EP/JP/FCC or customer-supplied guidelines.
- Typical testing may include dissolution, titration, polarimetry, loss on drying, viscosity, residue on ignition, heavy metal content, FTIR, HPLC, and GC.
- 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.
- Operate safely, 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.
Qualifications
- 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.
- Ability to assist with lifting of liquid containers and objects greater than 50 lbs.
- Ability to operate safely in a dynamic environment with mobile and fixed equipment and changing conditions while completing tasks ranging from simple to complex and/or multi‑tasking.
Benefits
- Several Employee Resource Groups focusing on diversity & inclusion.
- Tuition reimbursement – assistance to finish your degree or earn a new one.
- Generous 401K match.
- 152 hours accrued PTO plus 8 paid holidays.
Schedule
Typical working hours are Monday‑Friday, 3 PM – 11:30 PM.
We need to ensure we didn't duplicate schedule info (we already have in About the role). But we can keep schedule section with just the hours; the About the role also includes location and other details. It's okay to have some overlap? The instruction: Preserve ALL substantive information; do NOT invent or summarize away detail. It didn't forbid duplication, but better to avoid duplication. However schedule is already in About the role; we could remove schedule from About the role and keep only in Schedule section. But About the role also includes location and other details; we could keep schedule only in Schedule section and remove from About the role. Let's do that: About the role paragraph will not include schedule; we will put schedule in its own section. Thus About the role paragraph: remove the schedule sentence. Let's rewrite About the role: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.
Schedule section:Typical working hours are Monday‑Friday, 3 PM – 11:30 PM.
Now ensure we didn't lose any other substantive info: The "Typical working hours are Monday-Friday 3 PM - 11:30 PM." is now only in Schedule section. Good. Check other info: The "Catalent offers rewarding opportunities to further your career!" is vague; we omitted. The "Visit Catalent Careers to explore career opportunities." is boilerplate; omitted. The "personal initiative. dynamic pace. meaningful work." is vague; omitted. Now ensure we didn't miss any specifics: The "Assisting with other personnel with lifting of liquid containers and all objects of greater than 50 lbs." we captured as ability to assist with lifting. Good. "Operating safely in a dynamic environment which includes mobile and fixed equipment and changing conditions while completing job tasks that range from simple to complex and/or multi-tasking." captured. Now check if any other specifics: "The Role Perform efficient/reliable/high quality analytical testing in accordance with USP/NF/EP/JP/FCC/etc. or customer supplied guidelines." captured. "Typical testing may include Dissolution, Titration, Polarimetry, Loss on Drying, Viscosity, Residue on Ignition, Heavy Metal Content, FTIR, HPLC, and GC, etc." captured. "Maintain accurate written records of all analysis performed." captured. "Accurately interpret and effectively communicate analytical results and issues." captured. "Schedule daily tasks in an organized and efficient manner." captured. "Calibrate and maintain lab equipment and instrumentation." captured. "Responsible for operating in a safe manner, must be familiar with basic laboratory and chemical hygiene practices" captured. "Perform peer review of analytical testing and write up." captured. "Write SOPs on an as needed basis." captured. "Other duties as required in support of Catalent Pharma Solutions high performance" captured. Now the "Why You Should Join Catalent" section: we captured benefits: Employee Resource Groups focusing on D&I, Tuition Reimbursement, Generous 401K match, 152 hours accrued PTO + 8 paid holidays. Also "Catalent offers rewarding opportunities to further your career!" we omitted as vague. Also "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." That's substantive but maybe could be included in About the role or Benefits? It's a selling point; maybe we could add a paragraph under About the role or a separate