Regulatory Affairs Specialist applicants have rated the interview process at West Pharmaceutical Services with 2.5 out of 5 (where 5 is the highest level of difficulty) and assessed their interview experience as 25% positive. To compare, the company-average is 74% positive. This is according to Glassdoor user ratings.
Candidates applying for Regulatory Affairs Specialist roles take an average of 56 days to get hired, when considering 4 user submitted interviews for this role. To compare, the hiring process at West Pharmaceutical Services overall takes an average of 22 days.
Common stages of the interview process at West Pharmaceutical Services as a Regulatory Affairs Specialist according to 4 Glassdoor interviews include:
Phone interview: 27%
One on one interview: 18%
Skills test: 18%
Group panel interview: 9%
Background check: 9%
Drug test: 9%
Personality test: 9%
Here are the most commonly searched roles for interview reports -
I applied online. I interviewed at West Pharmaceutical Services (Chicago, IL)
Interview
The interview was straightforward, but they won't proceed due to a lack of sponsorship for the position. Unfortunately, sponsorship is unavailable for this role at the moment, hindering further progress.
I applied online. The process took 3 weeks. I interviewed at West Pharmaceutical Services (Exton, PA) in Apr 2024
Interview
I've made it into the second round with a manager, The interview process was normal and we discussed personal experiences, some information about the company's ongoing projects, and some behavior questions, But she was not very interested in my experiences and rejected me after the interview.
Interview questions [1]
Question 1
What do you know about our company?
Why did you leave your previous role?
I applied through an employee referral. The process took 3 months. I interviewed at West Pharmaceutical Services
Interview
Multiple round interview. First, was a phone interview with a recruiter. Then, I spoke with the hiring manager. Finally, I had a panel interview with 5 individuals via Microsoft Teams.
Interview questions [1]
Question 1
Describe your regulatory experience with the FDA submission and EU submissions. Which regions are you familiar with?