Top 25 Quality control lab Jobs in Easton Pa

Quality Control Data Reviewer 1st Shift
Quva Pharma —Bloomsbury, NJ
- $74,766 - $102,817 a year
- Overtime
- Microsoft Word
- Background check
- Microsoft Excel
- Paid holidays
- Health insurance
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13d
Manager, Quality Control Lab
QuVa Pharma —Bloomsbury, NJ
- $98,891 - $135,975 a year
- Full-time
- Background check
- Bachelor of Science
- 3 years
- Paid holidays
- Health insurance
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Quality Control Specialist I
OraSure Technologies Inc. —Bethlehem, PA
- $43,000 - $74,000 a year
- Overtime
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Free parking
- Disability insurance
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QA Inspector - C Shift 7:00am - 7:00pm
Pretium —Bethlehem, PA
- SQL
- Entry level
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Quality Assurance Inspector
Thermo Fisher Scientific —Allentown, PA
- $23 - $32 an hour
- 8 hour shift
- Mid-level
- High school diploma or GED
- 1 year
1d
Quality Lab Technician
Fabric Development Inc. —Quakertown, PA
- $19.50 an hour
- Full-time
- English
- High school diploma or GED
- Ability to lift 75 pounds
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QC Tech 2nd Shift - Bethlehem, PA
Kerry —Bethlehem, PA
- $22 - $32 an hour
- Full-time
- Computer literacy
- Pass drug screening
- Mid-level
- Health insurance
- Dental insurance
Quality Supervisor
Pretium —Bethlehem, PA
- Oracle
- Computer literacy
- Writing skills
- On-the-job training
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Quality Assurance Technician
Gregory Packaging —Bethlehem, PA
- Overtime
- Microsoft Word
- Ability to walk for extended periods
- Mid-level
- Paid holidays
- Health insurance
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QC Chemist I (Tues-Sat 8am-5pm)
B. Braun US Device Manufacturing LLC —Allentown, PA
- $70,000 - $78,300 a year
- Mid-level
- Master's degree
- Bachelor's degree
- Health insurance
- 401(k)
QC Analyst I
PPL Healthcare LLC —Sellersville, PA
- Full-time
- Bachelor's degree
- Continuous improvement
- Organizational skills
13d
QA Tech (3rd Shift)
Simmons Animal Nutrition, Inc —Quakertown, PA
- Microsoft Word
- Mid-level
- High school diploma or GED
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Quality Technician
Keystone Cement Company LLC —Bath, PA
- Full-time
- Microsoft Outlook
- Mid-level
- Ability to lift 50 pounds
- Health savings account
- Dental insurance
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23h
Principal Scientist, QC Compliance
Quva —Bloomsbury, NJ
- $113,754 - $177,695 a year
- Full-time
- Background check
- Master's degree
- Analysis skills
- Paid holidays
- Health insurance
Quick Apply
QA Inspector - A Shift 7:00am - 7:00pm
Pretium —Bethlehem, PA
- SQL
- Entry level
Quick Apply

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Quality Control Data Reviewer 1st Shift
Quva Pharma —Bloomsbury, NJ
B.S. degree or higher in Biology, or related field. Communicates as needed any testing issues to either a supervisor or manager or to a cross-functional group…
$74,766 - $102,817 a year
Quick Apply
13d
Quality Control Technician II
United Premium Foods, LLC —Woodbridge, NJ
Perform studies and analytical & statistical analysis to improve quality of products. Knowledge of Basic HACCP Principles or Experience working in an SQF (Safe…
$19 - $21 an hour
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Quality Control Data Reviewer 1st Shift

Quva Pharma -
Bloomsbury, NJ

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Job Details

Full-time
$74,766 - $102,817 a year
13 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
Vision insurance
401(k) matching
Opportunities for advancement

Qualifications

Pharmaceutical company experience

Full Job Description

Our Sterility Assurance Data Reviewer plays a vital role in ensuring the highest quality and safety standards of our pharmaceutical products. Once you complete our training, your responsibilities will include performing review of Sterility testing data for conformance to methods, SOPs, cGMP and Good Documentation Practices. Your attention to detail and adherence to precise procedures will guarantee that our medications meet the highest standards of safety, efficacy, and quality, providing patients with the best possible care and outcomes. Turn your passion for precision and your commitment to quality into a meaningful impact on healthcare across the US.

This is a full-time role, working Monday through Friday 6:00 AM - 2:30 PM. This is a set, consistent schedule with minimum overtime requirements and based on site in our Bloomsbury, NJ location. This is a safety sensitive position that may be subject to random drug testing, in accordance with applicable laws.

What the Quality Control Data Reviewer Does Each Day:

Reviews analytical testing of sterile products, and raw materials, following all written procedures and cGMP, and providing assurance of accurate documentation of analyses
Conducts and writes laboratory investigations, with support from the Manager
Verifies appropriate documentation for DEA controlled sample handling
Documents completion of review and approval of data in the appropriate laboratory systems
Reports any issues to the Supervisor upon discovery
Partners with their Supervisor to understand overall expectations and execute them independently based on the prioritization of projects
This individual will work with the Supervisor or Manager to understand overall expectations and provide data to meet project milestones
Reads and understands SOPs and follow policy, procedure, and applicable government regulations, such as current Good Manufacturing Practices (cGMP), DEA compliance, quality standards and safety requirements
Provides review of analytical data in a timely manner
Provides input to SOPs to enhance the efficiency of the laboratory
Keeps up to date on SOPs, cGMP, and current Good Documentation Practices (cGDP) requirements
Provides updates to the QC Microbiologists about priority testing such as stability and validation
Communicates as needed any testing issues to either a supervisor or manager or to a cross-functional group such as Metrology
Recommends to Supervisor or Manager improvements to analytical test methods or documentation

Our Most Successful Quality Control Data Reviewer:

Detail-oriented with strong verbal and written communications skills
Highly organized
Knowledgeable in Microsoft Word and Excel
Fulfills expectations, establishes sustainable relationships with team members, maintains effective and meaningful communication channels

Minimum Requirements for this Role:

18+ years of age
Able to successfully complete a drug and background check
B.S. degree or higher in Biology, or related field. Relevant experience can be substituted on a case by case basis
3 or more years of laboratory experience in the Pharmaceutical Industry
Able and willing to walk, stoop, stand, bend, and lift up to 50 lbs. throughout each shift, with or without reasonable accommodation
Must be currently authorized to work in the United States on a full-time basis; Quva is not able to sponsor applicants for work visas

Any of the Following Will Give You an Edge:

Experienced with microbiology testing such as sterility, endotoxin, growth promotion, and bioburden
Experienced with SampleManager

Benefits of Working at Quva:

Set, full-time, consistent work schedule
Comprehensive health and wellness benefits including medical, dental and vision
401k retirement program with company match
17 paid days off plus 8 paid holidays per year
National, industry-leading high growth company with future career advancement opportunities
The base compensation for this role is estimated to be within the range described below. The compensation offered may vary depending on relevant factors such as experience, skills, training, education, certifications, geographic location, and market conditions
Range: $74,766- $102,817 per Year

About Quva:

Quva is a national, industry-leading provider of compounded injectable medicines and software solutions that help power the business of hospital and health-system pharmacy. Quva Pharma produces and distributes injectable medicines required by health care providers and critical to patient care. Quva BrightStream partners with health-systems to analyze large amounts of data and through AI and machine learning, develops software solutions that turns the data into insights that are used to better run their pharmacy operation. Quva’s overall product and technology offerings help health-systems achieve greater value and deliver the highest-quality patient care.

Quva is an equal opportunity employer and is committed to creating and maintaining a work environment that is free from all forms of discrimination and harassment. Quva's Equal Opportunity Policy prohibits harassment or discrimination due to age, ancestry, color, disability, gender, gender expression, gender identity, genetic information, marital status, medical condition, military or veteran status, national origin, race, religious creed, sex (including pregnancy, childbirth, breastfeeding, and any related medical conditions), sexual orientation, and any other characteristic or classification protected by applicable laws. All employment with Quva is “at will.”

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.

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Refine Your Search

quality control lab jobs in easton pa

Quality Control Data Reviewer 1st Shift

Manager, Quality Control Lab

Quality Control Specialist I

QA Inspector - C Shift 7:00am - 7:00pm

Quality Assurance Inspector

Quality Lab Technician

QC Tech 2nd Shift - Bethlehem, PA

Quality Supervisor

Quality Assurance Technician

QC Chemist I (Tues-Sat 8am-5pm)

QC Analyst I

QA Tech (3rd Shift)

Quality Technician

Principal Scientist, QC Compliance

QA Inspector - A Shift 7:00am - 7:00pm

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