Placements Alley
Lonza
Quality Control Supervisor
Bristol, NH,
03222
Part Time, Full Time
$15.91 per hour
Posted 4 days ago
Apply Now
Actively Hiring
United States, Portsmouth (New Hampshire)
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Shift is Sunday Through Wednesday 8pm to 630
Check out this video about what a career at our Portsmouth NH facility could look like for you: Your Career with Lonza in Portsmouth, NH (youtube.com)
10 Hour Shifts Either Sunday through Wed or Wed Through Saturday(1st and 2nd shift)
The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza’s manufacturing demands.
A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Key Responsibilities:
Running test samples for in-process, lot release and stability studies
Reviewing assays
Writing quality records (Deviations, CAPA, Change Control) and test methods
Performs other duties as assigned
Key Requirements:
Bachelor's or associate Degree preferably in Microbiology, Biochemistry, or related science discipline
2-4 years industry experience preferably in a cGMP environment
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Experience using GMP Quality Systems such as: TrackWise, LIMS preferred
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Reference: R62865
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Shift is Sunday Through Wednesday 8pm to 630
Check out this video about what a career at our Portsmouth NH facility could look like for you: Your Career with Lonza in Portsmouth, NH (youtube.com)
10 Hour Shifts Either Sunday through Wed or Wed Through Saturday(1st and 2nd shift)
The QC Analyst will act as a team member of the Quality Control department to support production of in-process and final product drug lots for customers. They will also participate in quality testing for ongoing customer stability studies and provide on-time, high quality results to meet Lonza’s manufacturing demands.
A QC Analyst applies job skills and company policies and procedures to complete a variety of tasks. They will work on assignments that are semi-routine in nature where ability to recognize deviation from accepted practice is required and works on problems of moderate scope in which analysis of situation or data requires a review of identifiable factors.
Key Responsibilities:
Running test samples for in-process, lot release and stability studies
Reviewing assays
Writing quality records (Deviations, CAPA, Change Control) and test methods
Performs other duties as assigned
Key Requirements:
Bachelor's or associate Degree preferably in Microbiology, Biochemistry, or related science discipline
2-4 years industry experience preferably in a cGMP environment
Use of Microsoft Suites (Word, Excel, PowerPoint)
Use of Laboratory computer systems
Experience using GMP Quality Systems such as: TrackWise, LIMS preferred
Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.
Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.
Reference: R62865
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FAQ's
Find the answers for the most frequently asked questions below
Are you looking for job openings with Lonza near Bristol, NH, US? You'll find plenty of opportunities in nearby cities, including Bedford, NH, Candia, NH, Canterbury, NH, Dunbarton, NH, Weare, NH, Hooksett, NH, Amherst, NH, Belmont, NH, Chester, NH, Concord, NH, Derry, NH, Dover, NH, Exeter, NH, Gilmanton, NH, Goffstown, NH, Laconia, NH, Londonderry, NH, Loudon, NH, Newton, NH, Alton, NH. These locations offer remote jobs, part-time jobs, and full-time positions with Lonza. Check out current job listings in these cities to discover more employment opportunities and local jobs hiring now in your area.
If you're searching for companies hiring now in Bristol, NH, US, several top employers are offering a variety of job opportunities. These include Angi and more. Whether you're looking for entry-level positions, work-from-home jobs, or immediate hire roles, you'll find plenty of local job listings in Bristol, NH, US.
A Quality Control Supervisor typically requires a Bachelor's degree in a field related to engineering, science, or business administration. However, relevant work experience in quality control or a related field can sometimes be substituted for a degree. Some employers may prefer candidates with a Master's degree or professional certifications in quality management systems like Six Sigma or ISO.
A Quality Control Supervisor is responsible for overseeing the production process to ensure that the manufactured goods meet the required quality standards. They inspect products, analyze data, and implement corrective actions when necessary to maintain and improve product quality.
Supervisory controls, in the context of a Quality Control Supervisor role, refer to the management strategies and procedures implemented to oversee and direct the work of employees to ensure quality standards are met consistently. These controls may include inspection, documentation, training, and feedback mechanisms.
Quality control supervisors typically earn an average annual salary of around $65,000 in the United States, according to the U.S. Bureau of Labor Statistics. However, salaries can vary widely depending on factors such as location, industry, and level of experience.
A Quality Control Supervisor oversees the inspection of products or services to ensure they meet specified quality standards. This includes monitoring production processes, identifying defects, and implementing corrective actions when necessary. They may also train inspectors and review quality control procedures.
A Quality Control Supervisor is responsible for overseeing the production process to ensure that the manufactured products meet the required quality standards. They inspect products, analyze data, and implement corrective actions when necessary to maintain product quality. They also train and supervise quality control staff.
A Quality Control Supervisor is a professional responsible for overseeing the production process to ensure that the final products meet the company's quality standards. They often implement quality control systems, inspect products, and resolve any issues that may affect product quality.
A Quality Control Supervisor is a professional responsible for overseeing the quality of products or services within a company. They ensure that the company's products meet required standards by conducting inspections, implementing quality control processes, and resolving any issues that may arise. They often work closely with production teams to improve efficiency and product quality.
A Quality Control Supervisor is responsible for overseeing the production process to ensure that the final products meet the company's quality standards. This includes inspecting goods, implementing quality control procedures, and resolving any issues that may affect product quality. They also train staff on quality control practices and may collaborate with other departments to improve production processes.