1

Cmc In Biotech Jobs in Alabama (NOW HIRING)

Experience in the pharmaceutical/biotechnology industries preferred * Experience with environmental ... About Parexel Parexel FSP includes the CMC Operations group. We provide pharmaceutical and ...

Cmc In Biotech information

What is a CMC in biotech position?

A CMC (Chemistry, Manufacturing, and Controls) position in biotech involves overseeing the development, manufacturing, and quality control of biopharmaceutical products. Professionals in this role ensure that products meet regulatory standards and are produced consistently, often requiring knowledge of GMP regulations, process development, and analytical techniques.

What is the difference between Cmc In Biotech vs Formulation Scientist?

AspectCmc In BiotechFormulation Scientist
Required CredentialsBachelor's or Master's in Life Sciences, Good Manufacturing Practice (GMP) knowledgeBachelor's or Master's in Pharmacy, Chemistry, or related field; GMP experience
Work EnvironmentLaboratories, manufacturing facilities, regulatory settingsLaboratories, R&D departments, manufacturing units
Employer & Industry UsageBiotech companies, pharmaceutical firms, contract manufacturing organizationsPharmaceutical companies, biotech firms, contract labs

While both roles operate within the biotech and pharmaceutical industries, Cmc In Biotech focuses on Chemistry, Manufacturing, and Controls documentation and regulatory compliance, whereas Formulation Scientists primarily develop and optimize drug formulations. Cmc In Biotech professionals ensure regulatory submissions are complete, while Formulation Scientists work on creating effective drug delivery systems. Both roles often collaborate but serve distinct functions within the product development pipeline.

What is a CMC in biotech?

In biotech, CMC stands for Chemistry, Manufacturing, and Controls, which refers to the detailed documentation and processes involved in developing and producing a pharmaceutical product. CMC professionals ensure that manufacturing processes meet quality standards and regulatory requirements, often working with laboratory analysis, process validation, and compliance documentation.

What is the CMC department in biotech?

The CMC (Chemistry, Manufacturing, and Controls) department in biotech is responsible for developing, manufacturing, and ensuring the quality of biopharmaceutical products. It involves activities such as process development, validation, regulatory documentation, and quality control to ensure products meet safety and efficacy standards.
What are popular job titles related to Cmc In Biotech jobs in Alabama? For Cmc In Biotech jobs in Alabama, the most frequently searched job titles are:

Scientist III Microbiologist - FSP

Parexel

On-site

Full-time

Retirement, PTO

Re-posted 15 days ago


Parexel rating

8.2

Company rating: 8.2 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

28th of 73 rated research


Job description

When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We are looking to fill a microbiologist position working as a full-time employee of Parexel FSP on long-term assignment onsite at one of our clients in West Point, PA. This position offers full benefits, sick time, 401K, paid holidays, and paid time off. This position does not offer any sponsorship.

Qualifications

  • Bachelor's degree required; concentration in a scientific or applied discipline strongly preferred, with 3-5 years of experience in pharmaceutical microbiology related position required; or a MS with 1-2 years of experience

Required Skills and Experience

  • Solid microbiology foundation with experience in performing product testing

  • Proven technical writing skills (SOPs, protocols)

Desired Skills and Experience

  • Experience in the pharmaceutical/biotechnology industries preferred

  • Experience with environmental monitoring and water testing preferred

Responsibilities

MICROBIOLOGICAL PRODUCT ANALYSIS

  • Analyze samples and compile meaningful data

  • Perform Investigations and prepare/respond to CAPA (Corrective and Preventative Action)

  • Review, revise Test Procedures / Standard Operating Procedures

  • Ad Hoc work

  • Rotational on-call assignments

MICROBIOLOGICAL ACTIVITIES Include (but not limited to):

  • Receive, verify & Log in samples

  • MLT (Microbial Limits Testing)

  • Method Suitability testing

  • Endotoxin testing

  • Return templates and shipping paperwork when and where appropriate

  • Compile and trend data

  • Prepare and ship materials offsite for ID/testing (when applicable)

  • Environmental monitoring

  • Stock culture management and quality control of same

  • Biological indicator management

  • Bioburden testing

  • Water sampling

  • Microbiological media management and quality control of same

  • Sterilization activities

  • Research experiments as deemed appropriate by client management

  • Method Validation/Qualification

  • Other microbiological activities

  • Rotational on-call assignments for responding to alarms

CALIBRATIONS:

  • Execute "Before-Use" calibrations prior to performing testing

  • Review calibration data within the ELN (Electronic Laboratory Notebook)

  • Prepare and submit equipment for calibrations (offsite or onsite)

  • Complete calibration/PM paperwork

  • PROCAL Entries

GMP ACTIVITIES:

  • Prepare GMP documentation as requested by management

  • Perform laboratory sanitizations and ensure cleanliness of laboratory workspace

  • Perform equipment sanitizations (incubators / hoods / refrigerators)

  • Purchase supplies (GMP)

  • Prepare and send documents to Records Center

INVESTIGATIONS:

  • Initiate, facilitate, and perform Investigations and NOEs (Notice of Event-NOE) for Environmental samples [NOE for Microbiological Environment Event (MEN)]

  • Inform management of non-conforming events

AUDITS:

  • Participate in audits (Regulatory, In-house, Corporate)

  • Participate in self-inspections and safety inspections

  • Retrieve data when requested by Microbiology management

TRAINING:

  • Complete assigned training when required

  • Ensure training is complete prior to performing tasks

The role is intended to be a 40 hours per week position.

About Parexel

Parexel FSP includes the CMC Operations group. We provide pharmaceutical and biopharmaceutical companies with qualified and talented technical professionals to support the development and delivery of new therapies.

For results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement.

Come join us!

#LI-DK1

EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


What Parexel employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom


PAREXEL logo

About PAREXEL

Sourced by ZipRecruiter

Bring your Data Management expertise to Parexel's Strategic Partnerships. Although we work globally, each partnership we form is deeply personal. We are as dedicated to every aspect of our client's product development as they are - and work closely with client teams in true partnership to understand both challenges and opportunities. At Parexel we are focused on meeting customer and patient needs through collaborative partnership so that we get treatments into the hands of patients who need them most.

Industry

Pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Waltham, MA, US

Year founded

1983