As a Quality Assurance Specialist you will be responsible for documenting and auditing cGMP ... in the area of Active Pharmaceutical Ingredients (API) manufacturing or related industrial ...
As a Quality Assurance Specialist you will be responsible for documenting and auditing cGMP ... in the area of Active Pharmaceutical Ingredients (API) manufacturing or related industrial ...
QA Operations Specialist
Indianapolis, IN · On-site
$88K - $132K/yr
... in biotech pharmaceutical industry with environmental monitoring & cleanliness zones The pay range for this position at commencement of employment is expected to be between $88,000.00 and $132,000.00 ...
QA Operations Specialist
Indianapolis, IN · On-site
$88K - $132K/yr
... in biotech pharmaceutical industry with environmental monitoring & cleanliness zones The pay range for this position at commencement of employment is expected to be between $88,000.00 and $132,000.00 ...
Head of QA Operations (Assoc Dir level)
Indianapolis, IN · On-site
$138K - $257K/yr
Prior experience supporting aseptic pharmaceutical manufacturing operations. * In-depth knowledge of current GMPs, Quality Assurance, Quality Control, and applicable regulatory requirements and ...
Head of QA Operations (Assoc Dir level)
Indianapolis, IN · On-site
$138K - $257K/yr
Prior experience supporting aseptic pharmaceutical manufacturing operations. * In-depth knowledge of current GMPs, Quality Assurance, Quality Control, and applicable regulatory requirements and ...
QA Operations Specialist
Indianapolis, IN · On-site
$88K - $132K/yr
Functional Breadth * QA and QC experience in biotech pharmaceutical industry with environmental monitoring & cleanliness zones EEO Statement: The Novartis Group of Companies are Equal Opportunity ...
QA Operations Specialist
Indianapolis, IN · On-site
$88K - $132K/yr
Functional Breadth * QA and QC experience in biotech pharmaceutical industry with environmental monitoring & cleanliness zones EEO Statement: The Novartis Group of Companies are Equal Opportunity ...
Supervisor, Quality Assurance
Anderson, IN · On-site
$90 - $120/hr
... in the Dietary Supplements and/or pharmaceutical manufacturing industry with 3+ years in a ... Strong knowledge of FDA Quality Systems regulatory requirements and of standards quality assurance ...
Supervisor, Quality Assurance
Anderson, IN · On-site
$90 - $120/hr
... in the Dietary Supplements and/or pharmaceutical manufacturing industry with 3+ years in a ... Strong knowledge of FDA Quality Systems regulatory requirements and of standards quality assurance ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$77K - $106K/yr
Join our dynamic Quality Assurance team as a QA Senior Specialist - Supplier Quality, where you'll ... OR 10+ years of experience in supplier quality management within a pharmaceutical ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$77K - $106K/yr
Join our dynamic Quality Assurance team as a QA Senior Specialist - Supplier Quality, where you'll ... OR 10+ years of experience in supplier quality management within a pharmaceutical ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$90 - $130/hr
Join our dynamic Quality Assurance team as a QA Senior Specialist - Supplier Quality, where you'll ... OR 10+ years of experience in supplier quality management within a pharmaceutical ...
New
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$90 - $130/hr
Join our dynamic Quality Assurance team as a QA Senior Specialist - Supplier Quality, where you'll ... OR 10+ years of experience in supplier quality management within a pharmaceutical ...
New
QA Inspector
Indianapolis, IN · On-site
$29 - $44/hr
... in Biology, Chemistry, or other Life Science discipline and 1+ years of GMP pharmaceutical industry ... Excellent interpersonal and team skills; work independently and carry out QA decisions based on ...
QA Inspector
Indianapolis, IN · On-site
$29 - $44/hr
... in Biology, Chemistry, or other Life Science discipline and 1+ years of GMP pharmaceutical industry ... Excellent interpersonal and team skills; work independently and carry out QA decisions based on ...
QA Inspector
Indianapolis, IN · On-site
$29 - $44/hr
... in Biology, Chemistry, or other Life Science discipline and 1+ years of GMP pharmaceutical industry ... Excellent interpersonal and team skills; work independently and carry out QA decisions based on ...
QA Inspector
Indianapolis, IN · On-site
$29 - $44/hr
... in Biology, Chemistry, or other Life Science discipline and 1+ years of GMP pharmaceutical industry ... Excellent interpersonal and team skills; work independently and carry out QA decisions based on ...
Quality Manager Life Science Division
New Whiteland, IN · On-site
$90 - $130/hr
... and in compliance with the client quality standards for pharmaceutical distribution operations ... Assurance in conjunction with clients. * Interpretsand applies applicable GxP regulations/policies ...
New
Quality Manager Life Science Division
New Whiteland, IN · On-site
$90 - $130/hr
... and in compliance with the client quality standards for pharmaceutical distribution operations ... Assurance in conjunction with clients. * Interpretsand applies applicable GxP regulations/policies ...
New
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$77K - $106K/yr
... pharmaceutical industry. You'll be part of a collaborative team that values innovation, problem-solving, and continuous improvement in a fast-paced GMP environment. As the QA Senior Specialist ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$77K - $106K/yr
... pharmaceutical industry. You'll be part of a collaborative team that values innovation, problem-solving, and continuous improvement in a fast-paced GMP environment. As the QA Senior Specialist ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$74K - $102K/yr
... pharmaceutical industry. You'll be part of a collaborative team that values innovation, problem-solving, and continuous improvement in a fast-paced GMP environment. As the QA Senior Specialist ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$74K - $102K/yr
... pharmaceutical industry. You'll be part of a collaborative team that values innovation, problem-solving, and continuous improvement in a fast-paced GMP environment. As the QA Senior Specialist ...
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$74K - $102K/yr
... pharmaceutical industry. You'll be part of a collaborative team that values innovation, problem-solving, and continuous improvement in a fast-paced GMP environment. As the QA Senior Specialist ...
Quick apply
Senior QA Specialist, Supplier Quality
Fishers, IN · On-site
$74K - $102K/yr
... pharmaceutical industry. You'll be part of a collaborative team that values innovation, problem-solving, and continuous improvement in a fast-paced GMP environment. As the QA Senior Specialist ...
Quality Assurance Analyst
Fort Wayne, IN · On-site
Subsidiary Steel Dynamics Overview We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a ...
Quality Assurance Analyst
Fort Wayne, IN · On-site
Subsidiary Steel Dynamics Overview We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a ...
Quality Assurance Analyst
Fort Wayne, IN · Hybrid
Steel Dynamics We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a particular focus on ...
Quality Assurance Analyst
Fort Wayne, IN · Hybrid
Steel Dynamics We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a particular focus on ...
Quality Assurance Analyst
Fort Wayne, IN · On-site
$70 - $90/hr
Subsidiary Steel Dynamics Overview We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a ...
Quality Assurance Analyst
Fort Wayne, IN · On-site
$70 - $90/hr
Subsidiary Steel Dynamics Overview We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a ...
... Quality Assurance team ... This role will play a critical part in driving testing efficiency, improving repeatability within ...
... Quality Assurance team ... This role will play a critical part in driving testing efficiency, improving repeatability within ...
Quality Assurance Analyst
Fort Wayne, IN · Hybrid
SubsidiarySteel DynamicsOverview We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a ...
Quality Assurance Analyst
Fort Wayne, IN · Hybrid
SubsidiarySteel DynamicsOverview We are seeking a Quality Assurance Analyst to assist in establishing our QA initiatives and team members. This position will help build out our QA processes with a ...
Quality Assurance Inspectors
Goshen, IN · On-site
Goshen IN Company: Keystone RV More about this job > Description We are looking for Quality Assurance inspectors to join our team. Keystone RV is a fast paced manufacturing company producing the most ...
Quality Assurance Inspectors
Goshen, IN · On-site
Goshen IN Company: Keystone RV More about this job > Description We are looking for Quality Assurance inspectors to join our team. Keystone RV is a fast paced manufacturing company producing the most ...
QA Analyst
Indianapolis, IN · On-site
Job ID: 804257 Job Title: QA Analyst Location: 550 W 16th Street Indianapolis IN 46202 Duration:12 + Months (Possibility of Extensions) Client: IDOH * Works with developers and chemists to ensure ...
Quick apply
QA Analyst
Indianapolis, IN · On-site
Job ID: 804257 Job Title: QA Analyst Location: 550 W 16th Street Indianapolis IN 46202 Duration:12 + Months (Possibility of Extensions) Client: IDOH * Works with developers and chemists to ensure ...
Quality Assurance In Pharmaceutical information
What does a quality assurance professional do in the pharmaceutical industry?
What are the key skills and qualifications needed to thrive as a quality assurance professional in the pharmaceutical industry?
What are some common challenges faced by quality assurance professionals in the pharmaceutical industry, and how can they be effectively managed?
What is the difference between Quality Assurance In Pharmaceutical vs Quality Control In Pharmaceutical?
| Aspect | Quality Assurance In Pharmaceutical | Quality Control In Pharmaceutical |
|---|---|---|
| Focus | Processes, compliance, and preventing defects | Testing and inspecting products for defects |
| Responsibilities | Developing quality systems, audits, documentation | Sampling, testing, and analyzing products |
| Credentials | GMP certifications, quality management training | Lab certifications, analytical testing skills |
| Work Environment | Office-based, quality departments, manufacturing sites | Laboratories, manufacturing facilities |
Quality Assurance In Pharmaceutical focuses on establishing and maintaining quality systems to prevent issues, while Quality Control In Pharmaceutical emphasizes testing products to identify defects. Both roles are essential in ensuring pharmaceutical safety and compliance, but they differ in scope and daily tasks.
Is quality assurance a good career in the pharmaceutical industry?
What does quality assurance do in the pharmaceutical industry?
What are popular job titles related to Quality Assurance In Pharmaceutical jobs in Indiana?
For Quality Assurance In Pharmaceutical jobs in Indiana, the most frequently searched job titles are:
What job categories do people searching Quality Assurance In Pharmaceutical jobs in Indiana look for?
The top searched job categories for Quality Assurance In Pharmaceutical jobs in Indiana are:
What cities in Indiana are hiring for Quality Assurance In Pharmaceutical jobs?
Cities in Indiana with the most Quality Assurance In Pharmaceutical job openings:

$58K - $71K/yr
Full-time
Posted 13 days ago
Job description
As a Quality Assurance Specialist you will be responsible for documenting and auditing cGMP practices for the site. The position develops and revises QA procedures to strengthen cGMP compliance as per the USFDA Title 21 Code of Federal Regulation Part 210, 211 and Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients.
Key Responsibilities:
- Acts as departmental resource for cGMP manufacturing programs.
- Work collaboratively with all departments to ensure manufacturing programs are delivered on time.
- Make and act upon GMP decisions.
- Writes, reviews and/or approves SOPs and other compliance documents for cGMP programs.
- Reviews and authorizes batch production records and quality control documentation.
- Sets-up and tracks material flow and material-labeling process to ensure compliance with cGMP program.
- Collaborate and interact internally to support the highest quality customer service.
- Acts a liaison between Avecia and client with respect to compliance in cGMP manufacturing programs.
Required Skills/Abilities:
- BS/BA in science with 1-3 years Quality Assurance cGMP experience or an Associate degree with 5+ years of Quality Assurance cGMP experience in the area of Active Pharmaceutical Ingredients (API) manufacturing or related industrial experience.
- High level of knowledge in cGMP guidelines as specified in ICH Q7A.
- Experienced at writing and reviewing GMP documents.
- Solves complex, non-routine analytical problems.
- Very strong oral and written communication skills.
The annualized salary range for this position is between $58,100.00 - $71,100.00.
About NITTO DENKO
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
51 - 200 Employees
Headquarters location
San Diego, CA, US