Boehringer Ingelheim

Automation Engineer | Staff / non-line Manager | MIRAI Program Group, Yamagata Plant (Higashine, Japan, Yamagata)

Higashine, Japan Type not listed
Manufacturing & CMC Manager

Boehringer Ingelheim 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

Responsibilities

Shall monitor and review all FEL3  and EPC  contractor’s technical work.

Monitor the development of engineering strategies, procedures and work processes.

Identify and implement, cost saving and optimization opportunities.

Engineering standardization, quality, time, cost and safety benchmarking.

A value engineering program.

Integrated operating plan for the Project including plant interconnection, start-up sequence, operating and shutdown philosophies.

Optimization of infrastructure, offsites and utilities.

Project and process design conditions standards and codes, Japan and BI-requirements for design, execution, documentation, permitting and operation.

Quality standards and procedures.

Safety, Health and Environmental codes, standards and regulations.

Understand Numbering systems for plant areas and equipment items, piping and instrumentation items, roads, buildings and all documentation.

Carry out verification of the basic design criteria, Project and engineering design bases, process and utilities requirements etc. so that work can then proceed on developing the Engineering package and other early engineering requirements.

Provide input for front end studies, reports etc, and basic engineering design for offsites, utilities and infrastructure areas, including preparation of technical scope of work for potential EPC contractors to bid for and carry out detailed engineering of these areas.

Strategic studies supporting Client and/or FEL3 contractor in decision making processes.

Review all FEL3 engineering documents such as Process Flow Diagrams, P&ID’s, plot plans, hazardous area classification, One Line Diagrams, Building arrangements and design, etc.

Review contractor's provision of process and mechanical data sheets for equipment items, including any input by specialist suppliers.

Review all relevant equipment items indicated by Technology Providers, process designers, etc. through design development. requisition, and enquiry, vendor selection through manufacture, ongoing inspection, completion, testing release from vendors' works and installation.

Review equipment for compliance with the specifications, and review Vendor drawings as necessary and EPC contractor's comments and check that comments are being incorporated.

Review EPC contractor's calculated utility consumption / production figures and compare to utility balances developed during FEL3 to verify that utility plant capacities are adequate.

Review EPC contractor's updated material balances of effluent streams and compare to material balances developed during FEL3. Verify that effluent treatment plant capacity is adequate, and that FEL3 and EPC contractor's designs comply with environmental requirements set out in the specifications.

Review all detailed engineering work by specialist disciplines to verify that it is developed in accordance with the specifications.

Review any FEL3 or EPC contractor requests to deviate from the Project standards and specifications, including resolving any conflicts between the standards, codes or specifications etc., and also review any FEL3 or EPC contractor additional specifications.

Review FEL3 and EPC contractor’s engineering for compliance with requirements of ARL Technology.

Participate in all design reviews including HAZOPs and other Safety Reviews. Model Reviews, etc. with Vendors, EPC contractor and Client as required.

Review all critical engineering documents when issued and check other documents in accordance with the guidelines set out in the various Agreements with respect to document review by Client .

Review technical content of claims for changes in the work.

Monitor production of Design Books, Operating Manuals and Catalogues of Vendor information, etc.

Ensure that the handover of engineering documents on the selected Electronic Data Management System (EDMS) format is both readily usable and accessible by Client.

Minimum Education/Degree Requirements

Degree/Education:

Bachelor’s degree

Focus:

Control and Automation, Electro-Electronic or Electrical Engineer or related fields

Required Capabilities (Skills, Experience, Competencies)

Language:

- English: Advance level (read, write and speak).

- Japanese: Advance level (read, write and speak).

Work Experience:

- Over 3 years of Automation Experience

- Pharmaceutical knowledge is desirable.

- Experience on international collaboration and project execution is desirable.

Soft Skills:

- Teamwork

- Proactive and Creative

- Communication and Good Relationship

- Focus on Customer

- Ownership

- Resilience

- Organization

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Job details

Seniority
Manager
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Higashine, Japan
Employment type
Not listed

How this role compares

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

We currently track 276 comparable Manager Manufacturing & CMC roles across 50 biopharma companies.

276Comparable roles tracked
256Currently active
50Companies hiring similar roles
23Countries represented

Salary context

95 of 276 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Operator - 2nd Shift · Mylan Technologies, Inc. $30,000/yr – $49,000/yr
Highest disclosed · Associate Director Packaging Development · Gilead Sciences, Inc. $182,070/yr – $235,620/yr
Peer group range $39,500 – $208,845 (median $169,000)

Where these roles are based

Top locations among the 276 comparable roles

United States172
India39
Ireland14
Singapore7
China's Mainland6
Netherlands5

+ 17 more countries

Seniority mix

276 of 276 peers have a known seniority level

Manager164
Associate68
Associate Director44

Therapeutic area mix

0 of 276 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

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.

60%similar
GlaxoSmithKline K.K. Akasaka, Japan Manager
Same function Same seniority Same country
60%similar
Amgen K.K. Tokyo, Japan Manager
Same function Same seniority Same country
60%similar
Boehringer Ingelheim Higashine, Japan Manager
Same function Same seniority Same country
45%similar
Lilly Cork, Cork, Ireland Manager
Same function Same seniority
45%similar
AbbVie Manager
Same function Same seniority

Open in 4 locations

North Chicago, United StatesIrvine, United StatesSouth San Francisco, United StatesWorcester, United States
45%similar
AbbVie North Chicago, IL Manager
Same function Same seniority

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.

60%
Japan Site Planning Manager
GlaxoSmithKline K.K. · Akasaka, Japan · Manager
Function Therapeutic area Seniority Country
45%
Sr. Associate/Manager - Global CMC Regulatory Associate
Lilly · Cork, Cork, Ireland · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager, Product Development Quality Assurance (CMC Product Lead)
AbbVie · South San Francisco, CA · Manager
Function Therapeutic area Seniority Country
45%
Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC)
AbbVie · Waltham, MA · Manager
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.