Roche Posted August 25, 2026

Production Technician (3rd shift)

Indianapolis, Indiana, United States of America FULL_TIME
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This position is no longer accepting applications.

Roche has closed or removed this posting -- see current similar openings below.

View the original listing (may no longer be live).

About this opportunity

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Roche.

As a Production Technician, you will have key responsibilities supporting manufacturing operations either in the manufacturing, packaging, and/or product labeling areas. You will set up and operate a variety of automatic or semi-automatic machines used in the production of the company's product. You will work from process sheets or written/verbal instructions given by the supervisor to perform production tasks. You will also check and inspect operations against predetermined tolerances. You will provide support to an area, person, or program. Interface with internal customers. Perform semi-routine support duties of a specialized nature within an assigned area. You will also be responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions.

The opportunity:

Maintaining material/supply needs to support production.

Setting up & operating equipment and processing materials & packaging kits in accordance with standard operating procedures.

Inspecting products and components to verify completeness of the final device and product information is precise and legible. Inspecting product for quality and adherence to specifications

Ensuring full compliance with both GMP and housekeeping standards within packaging area.

Participating in trouble-shooting and problem solving associated with packaging process.

Completing and ensuring accuracy of all process orders and associated required documentation, records, and metrics.

Preparing work centers for appropriate line clearance procedure and conducting regular cleaning in accordance with standard operating procedures.

May train others in department as needed.

Who you are:

Minimum Qualifications:

High School Diploma or equivalency.

Ability to read and speak English.

Strong interpersonal skills and the ability to work in a team environment.

Ability to learn multiple jobs and responsibilities, and adjust between them as needed.

Ability to work in a fast paced environment.

Preferred Qualifications:

1 year of related experience in production or manufacturing assembly in a regulated industry.

Ability to lift up to 35 lbs. occasionally.

Ability to have flexibility in work schedule when needed.

Basic computer skills with competency using standard software packages.

Thorough understanding of the principles and applications of Good Manufacturing Practices (GMP) and ISO.

Ability to perform basic mathematical calculations.

Thorough understanding of appropriate safety procedures.

Detail oriented.

Relocation benefits are not available for this job posting.

Pay transparency

The expected salary range for this position based on the primary location of Indianapolis is $36,300.00 - $67,500.00 Annual. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.  A discretionary annual bonus may be available based on individual and Company performance.  This position also qualifies for the benefits detailed at the link provided below.

Benefits

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants .

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Indianapolis, Indiana, United States of America
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 2526 comparable Manufacturing & CMC roles across 157 biopharma companies.

2526Comparable roles tracked
2230Currently active
157Companies hiring similar roles
61Countries represented

Salary context

639 of 2526 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 Not listed on this posting
Lowest disclosed · Sr Manufacturing Technician · Genz. Therap Product LP $2,400/yr – $3,200/yr
Highest disclosed · Executive Director, CMC Regulatory Science · ModernaTX, Inc. $224,900/yr – $404,600/yr
Peer group range $2,800 – $314,750 (median $122,900)

Where these roles are based

Top locations among the 2526 comparable roles

United States1157
India165
Germany152
Switzerland89
France89
Netherlands87

+ 55 more countries

Seniority mix

1056 of 2526 peers have a known seniority level

Senior320
Manager267
Associate129
Principal99
Associate Director90
Director86
Senior Director33
Intern/Fellow/Postdoc26
Executive/VP6

Therapeutic area mix

5 of 2526 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Rare Disease2
Vaccines & Infectious Disease1
Oncology1
Respiratory1

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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.

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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.