Manufacturing Technician - Weekend Shift
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Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.
Job Description
Carry out daily tasks as assigned by the Production Manager according to GMP and the quality system.
Active involvement and management of batch related CAPA’s as they arise in the business unit taking them from the initial review state through RCA, approval, batch disposition and delivery of corrective and preventive actions, liaising closely with the relevant Departments and QA Lead to ensure thorough investigation is completed and timely resolution and closure is met.
Accurately completing documentation in a timely manner, accurately and legibly.
Responsible for maintaining & monitoring grade A conditions inside isolator, including end of batch EM and utilizing the FMS system for data collection and completing glove testing for integrity of RAB units.
Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies.
Competent in surface sanitization and use of qualified Disinfectants/Detergents/Biocide cleans, competent in both SIP sterilization & bespoke autoclave counter pressure training.
Manage requirements in order to deliver the KPIs as they relate to the Product Flow function with a specific emphasis on the 32 day release cycle
Adhering to all company standards in safety, housekeeping and quality, notifying management of any discrepancies.
Follow gowning procedures on entry to areas and donning additional garbing for specific tasks within the compounding area.
Adhere to and support all EHS & E standards, procedures, and policies.
Qualifications
Understanding of the requirements to work in a regulated GMP industry
Ability to build strong relationships and work within cross-functional teams.
Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
Drive, high energy, maturity, and ability to work under pressure, deliver results, and overcome obstacles.
Team player who can collaborate with others to achieve organizational targets and goals.
Knowledge of biologics operations an advantage
Excellent communication skills
Ability to use sound judgment to make effective decisions within appropriate timeframes
Proven to be self-directed, self-motivated and ability to prioritize competing priorities
Excellent technical writing skills is a requirement for this role and previous experience on GTW i.e. opening RCC’s / LIRs / CAPA’s is preferrable in order to be successful within this role
2-3 Years working in a manufacturing environment, preferably Aseptic/Sterile Manufacturing.
Experience working in a cleanroom environment.
Third Level qualification in science or engineering discipline is an advantage but not essential.
Ability to build strong relationships and work within cross-functional teams.
Adaptability to work in a fast, dynamic environment whilst adjusting readily to meet unexpected constraints.
Additional Information
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 2556 comparable Manufacturing & CMC roles across 173 biopharma companies.
Salary context
663 of 2556 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 2556 comparable roles
+ 50 more countries
Seniority mix
1172 of 2556 peers have a known seniority level
Therapeutic area mix
12 of 2556 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.