Novartis Posted October 27, 2026

Production Technician

Indianapolis, United States FULL_TIME
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Novartis is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

As a Production Technician, you will play an active role in the daily production of isotopes used in advanced radioligand therapies while supporting the setup, preparation, and operation of equipment and manufacturing systems. Working as a qualified radiation worker in a controlled manufacturing environment, you will execute production activities in accordance with batch records, standard operating procedures, and regulatory requirements. Partnering closely with Production Leads and Managers, you will help ensure manufacturing operations are performed safely, efficiently, and on schedule while contributing to therapies that help transform outcomes for patients.

#LI-OnsiteShift: Monday - Friday 3rd ShiftNOTE: This is a 3rd shift role.  Hours are expected to be 10 pm – 6 am, Monday – Friday. Shift schedules may change based on business need.  Location: Indianapolis, IN, United StatesRelocation Support: This role is based in Indianapolis, IN, United States. Novartis is unable to offer relocation support: please only apply if accessible.Key ResponsibilitiesExecute manufacturing activities for isotope products in accordance with batch records and established procedures.Operate and maintain Grade C isolators while supporting safe, compliant production operations.Follow radiation safety requirements, including dosimetry, personal protective equipment, and ALARA principles.Perform contamination control, personnel monitoring, and material monitoring in accordance with site procedures.Support production readiness through equipment cleaning, sterilization, and preparation of manufacturing areas.Conduct routine and dynamic environmental monitoring to maintain manufacturing readiness and compliance.Prepare, verify, and maintain materials in accordance with defined batch monitoring procedures.Participate in qualification and validation activities to support operational readiness and process compliance.Complete production documentation, including batch records, shipping documents, and training records.Support a culture of safety, quality, current Good Manufacturing Practice compliance, and open communication within the manufacturing team.Essential RequirementsHigh school diploma or equivalent required; Bachelor's degree in a scientific discipline strongly preferred.Minimum 2 years of experience in a current Good Manufacturing Practice or aseptic manufacturing environment.Minimum 2 years of pharmaceutical manufacturing experience; low-bioburden manufacturing experience preferred.Knowledge of current Good Manufacturing Practice regulations and regulated manufacturing environments.Ability to work safely with radioactive materials in a controlled manufacturing environment.Experience following standard operating procedures, batch records, and manufacturing documentation.Ability to wear cleanroom garments, personal protective equipment, and required respiratory protection.Strong attention to detail, communication skills, and commitment to safety, quality, and compliance.Desirable RequirementsTraining in radiochemistry or radiopharmacy strongly preferred.Hands-on experience in radiochemistry, isotope production, or radiopharmaceutical manufacturing with radioactive materials in a Good Manufacturing Practice environment strongly preferred.Languages:EnglishThe salary for this position is expected to range between $25.19 and $46.82 per hour. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves. To learn more about the culture, rewards and benefits we offer our people click here.

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Indianapolis, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 3374 comparable Manufacturing & CMC roles across 173 biopharma companies.

3374Comparable roles tracked
3074Currently active
173Companies hiring similar roles
61Countries represented

Salary context

792 of 3374 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.

This roleSubject $25/hr – $47/hr (≈ $52,395–$97,386/yr)
Lowest disclosed · Operator – Plant Utilities · Lilly $13/hr – $28/hr (≈ $26,998–$58,302/yr)
Highest disclosed · Head of Analytical Development · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $42,650 – $381,150 (median $128,400)

Where these roles are based

Top locations among the 3374 comparable roles

United States1531
Germany216
India155
France145
Ireland130
China121

+ 55 more countries

Seniority mix

1484 of 3374 peers have a known seniority level

Senior403
Manager351
Intern/Fellow/Postdoc198
Associate142
Principal126
Director106
Associate Director104
Senior Director47
Executive/VP7

Therapeutic area mix

21 of 3374 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease13
Rare Disease3
Oncology2
Dermatology & Aesthetics1
Respiratory1
Immunology1

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.

40%similar
40%similar
Lilly Indianapolis, Indiana, United States of America Director
Same function Same country
40%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function Same country
40%similar
Merck West Point, Pennsylvania, United States of America Principal
Same function Same country
40%similar
Merck West Point, Pennsylvania, United States Intern/Fellow/Postdoc
Same function Same country
40%similar
AbbVie North Chicago, IL Associate Director
Same function Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Manufacturing & CMC job in the United States, and choose locations and companies.

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.

40%
Director, Global Regulatory Affairs – Chemistry, Manufacturing and Controls (CMC), Platform Innovation – Synthetic Peptides and Oligonucleotides
Lilly · Indianapolis, Indiana, United States of America · Director
Function Therapeutic area Seniority Country
40%
Associate Principal Scientist/Engineer, Medical Device and Combination Products, Analytical
Merck · West Point, Pennsylvania, United States of America · Principal
Function Therapeutic area Seniority Country
40%
Senior Scientist II - Biologics Drug Product Development
AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
40%
Senior Scientist I - Peptide Analytical Chemistry
AbbVie · North Chicago, IL · Senior
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 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.